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US3198826A - Alkyl mercaptomethylphosphonic acids - Google Patents

Alkyl mercaptomethylphosphonic acids
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Publication number
US3198826A
US3198826AUS305809AUS30580963AUS3198826AUS 3198826 AUS3198826 AUS 3198826AUS 305809 AUS305809 AUS 305809AUS 30580963 AUS30580963 AUS 30580963AUS 3198826 AUS3198826 AUS 3198826A
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US
United States
Prior art keywords
acid
alkyl
additive
mineral oil
oil
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US305809A
Inventor
George M Calhoun
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Shell USA Inc
Original Assignee
Shell Oil Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to NL272804DpriorityCriticalpatent/NL272804A/xx
Priority to BE611851Dprioritypatent/BE611851A/xx
Priority to BE626579Dprioritypatent/BE626579A/xx
Priority to NL250415Dprioritypatent/NL250415A/xx
Priority to NL272803Dprioritypatent/NL272803A/xx
Priority to NL109943Dprioritypatent/NL109943C/xx
Priority to NL287245Dprioritypatent/NL287245A/xx
Priority claimed from US805686Aexternal-prioritypatent/US3112271A/en
Priority to FR824022Aprioritypatent/FR1253771A/en
Priority to DES68011Aprioritypatent/DE1151085B/en
Priority to GB12814/60Aprioritypatent/GB904968A/en
Priority claimed from US77830Aexternal-prioritypatent/US3112269A/en
Priority claimed from US77817Aexternal-prioritypatent/US3238131A/en
Priority to FR882716Aprioritypatent/FR81903E/en
Priority to GB45905/61Aprioritypatent/GB955357A/en
Priority to GB45909/61Aprioritypatent/GB1010536A/en
Priority to FR882715Aprioritypatent/FR81706E/en
Priority claimed from US162924Aexternal-prioritypatent/US3226322A/en
Priority claimed from US183036Aexternal-prioritypatent/US3232882A/en
Priority to FR919847Aprioritypatent/FR83758E/en
Priority to GB48702/62Aprioritypatent/GB957772A/en
Priority to US305809Aprioritypatent/US3198826A/en
Application filed by Shell Oil CofiledCriticalShell Oil Co
Priority to US312329Aprioritypatent/US3316332A/en
Priority to US472663Aprioritypatent/US3309428A/en
Publication of US3198826ApublicationCriticalpatent/US3198826A/en
Application grantedgrantedCritical
Anticipated expirationlegal-statusCritical
Expired - Lifetimelegal-statusCriticalCurrent

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United States Patent 3,193,626 ALKYL MERQAPTQN THYLPHOSPHGNIC ACIDS George M. Calhoun, Cleveland, Ghio, assignor to Shell Gil Company, a corporation of Delaware No Drawing. Original application Apr. 13, 1959, Ser. No. 895,686, new Patent No. 3,112,271, dated Nov. 26, 1963. 'Divided and this application Aug. 39, 1963,
Ser. No. 305,809
2 Claims.
This patent application is a division of copending patent application Serial No. 805,686, filed April 13, 1959, and which matured on November 26, 1963, into US. Patent 3,112,271.
This invention relates to a new and novel class of organic Z-thia-methyl phosphono compounds. More particularly the invention is directed to esters of 2-thiamethyl phosphonic acid and their use as additives in various organic compositions such as oils, plastics, etc.
The invention is directed to 2-thia-alkyl phosphoruscontaining compounds having the general formula:
wherein R is a hydrocarbyl radical having at least 6 carbon atoms such as a saturated C1048 alkyl radical, or an arakyl or aryl radicals; the R s are the same or different C alkyl radicals or hydrogen, or amine, preferably an alkyl amine. Preferred compounds of the general Formula I have the following formula:
and of the above formulas it is preferred that the alkyl portion of the molecule be C1048 alkyl and wherein R is hydrogen or a short alkyl radical of 1-4 carbon atoms, A is an aliphatic amine, preferably a primary or secondary amine, such as C primary straight chain amines, e.g., octylamine, laurylamine, stearylamine, etc., or branched chain primary aliphatic amines, e.g., t-C alkylamine, such as t-c H17NH2, t-C H NH to ttCfiHgjNHg 0r C5 13 secondary aiiphatic amines, such as diamylamine, di-Z-ethylhexylamine, didecylamine, etc.
The Z-thiaalkylphosphonic compounds are prepared by reacting a mercaptan or mercaptide having at least 6 carbon atoms with a halomethylphosphono compound such as chloromethylphosphonic acid or chloromethylphosphonate or their thioderivatives in a suitable solvent, such as an aqueous alcoholic solution, at reflux temperature and under inert conditions until the reaction is completed which normally requires from 1 to about 5 days. The mercaptans include aliphatic mercaptans, such as hexyl, octyl, decyl, dodecyl, octadecyl mercaptans, cycloalkyl mercaptans, such as cyclohexyl mercaptan, dicyclohexyl mercaptan, aralkyl mercaptan;
such as phenyldecyl mercaptan, benzyl mercaptan and the like. Instead of the mercaptans, the mercaptides can be used such as the alkali metal (Na or K) mercaptides of the above compounds. Suitable halomethylphosphonic compounds include chloromethylphosphonic acid, mono or dihydrocarbyl chloromethylphosphonates, e.g., mono or dibutylv chloromethylphosphonate, mono or di-Z-ethylhexyl chloromethylphosphonate, mono or dilauryl chloromethylphosphonate, mono or diphenyl chloromethylphosphonate, mono or dicyclohexyl chloromethylphosphonate, mono or dibenzyl chloromethylphosphonate, dibutyl dithiochloromethylphosphonate, diphenyl chloromethyl dithiophosphonate, dibutyl chloromethyltrithiophosphonate, alkali metal salts such as Na and K salts of chloromethylphosphonic acid, Na and K salts of monobutyl chloromethylphosphonic acid, Na and K salts of monodecyl chloromethylphosphonic acid and the like.
'A preferred method of making the 2-thiaalkylphos phonates is to react a suitable mercapto compound, such as an alkali metal (Na or K) C1048 alkyl mercaptide with an alkali metal (Na or K) saltof chloromethylphosphonic acid in an alcoholic solution under reflux conditions and under an inert atmosphere to form the alkali metal salt of an alkylmercaptomethylphosphonic acid. The salt is then treated with a strong acid such as hydrochloric acid to spring the free alkylmercaptomethylphosphonic acid, which can be converted into desired partial or full esters of polyvalent metal salts or amine salts for use as oil, fuel and grease additives as well as other uses.
The following examples illustrate the preparation of additives for use in accordance with the present invention.
EXAMPLE I Stoichiometric amounts of the potassium salt of decyl mercaptan and monochloromethylphosphonic acid were dispersed in an aqueous solution of ethyl alcohol and the mixture was refluxed at 78 C. under a nitrogen atmosphere for about 1 day. The potassium decylmercaptomethylphosphonate was then treated with strong hydrochloric acid to spring the free phosphonic acid which was recovered by extraction with ether. The final product decylrnercaptomethylphosphonic acid analyzed as follows:
The procedure of Example I was followed except that potassium salt of phenylmercaptanwas used instead of potassium salt of decylmercaptan and the final product was phenylmercaptomethylphosphonic acid.
EXAMPLE In The dibutyl ester of decylmercaptornethylphosphonic acid of Example I was prepared by treating decylmercaptomethylphosphonic acid with butyl alcohol in an alcoholic solution at about and extracting the ester with ether. 7 1
EXAMPLE IV Di-Z-ethylhexylamine vsalt of decylmercaptomethylphosphonic acid (Z-thiadodecylphosphonic acid) was prepared by reacting the product of Example I with di-2- ethylhexylarnine in an amount sufiicient to completely Fatented Aug. 3, 1965 i neutralize both acid groups, at about 50 C. in an alcoholic solution and thereafter recovering the amine salt from the alcoholic solution.
EXAMPLE V Following the procedure of Example IV, the tert-octadecylamine salt of decylmercaptomethylphosphonic acid -was prepared using tert-octadecylamine, available commercially under the trade name of Primeme J M-R, instead of di-Z-ethylhexylamine.
The following additional compounds were prepared: octylmercaptomethylphosphonic acid, dodecylmercaptomethylphosphonic acid, cyclohexylmercaptomethylphosphonic acid, benzylmercaptomethylphosphonic acid, phenylmercaptomethylphosphonic acid, dibutyl decylmercaptomethylphosphonate, phenyldecylmercaptomethyl acid phosphonate, dithiobutyl dodecylmercaptomethylphosphonate, dibutyl phenylmercaptomethylphosphonate, phenyldecylmercaptomethyl acid phosphonate, dithiobutyl dodecylmercaptomethyphosphonate, dibutyl phenylmercaptomethylphosphonate, dithiooctyl cyclohexylmercaptomethylthiophosphonate, dioctylamine dodecylmercaptomethylphosphonate, dioctadecylamine phenylmercaptomethylphosphonate, tert-octadecylamine dodecylmercaptomethylphosphonate and mixtures thereof.
The additives of this invention are novel compounds. They are oil-soluble and can be used in amounts of from about 0.1% to about 25%, preferably from about 0.5%
'to about 5.0% by \weight.
Mercaptomethylphosphono compounds of this invention are outstanding additives for various liquid hydrocarbon products, such as natural and synthetic hydrocarbon lubricating oils, greases, fuels (gasoline, kerosene, gas oil, burner fuel oil), asphalts, waxes, slushing oil, industrial oils, e.g., metal working and drawing oils, quenching oils, textile oils, hydraulic oils, dielectric compositions and other industrial oils. They are particularly outstanding when added in small amounts to lubricating oils and lubricating compositions to impart extreme pressure and anti-wear properties to such materials. Also, these additives are useful additives for gasoline, fuel oils, and other light oil products.
The following compositions are illustrative of the invention, the percentages being by weight, of the indicated additive or additives with the remainder being essentially the base.
Composition A: Percent Example I additive 2 1010 mineral oil Balance Composition B:
Example II additive 2 1010 mineral oil Balance Composition C:
Example III additive 2 1010 mineral oil Balance Composition D:
Example IV additive 2 1010 mineral oil Balance Composition E:
Example II additive 1 SAE 30 mineral oil Balance Composition F:
Example I additive 2 SAE 90 mineral oil Balance Composition G:
Example I additive 2 Laurie acid 2 SAE 90 mineral oil Balance Composition H:
Example I additive 5 'Ucon 50HB660 (polyethylene propylene glycol having a SUS viscosity at 100 F.
of 660) Balance 4 Composition I:
Example I additive 2 Di-Z-ethylhexyl sebacate Balance Composition .1
Example I additive 1 Leaded gasoline (3 cc. of TEL) Balance Composition K:
Example I additive 0.1 Fuel oil (No. 2) Balance Compositions of this invention were evaluated for their extreme pressure properties on a Spur-Gear machine. The machine consists essentially of two geometrically similar pairs of gears connected by two parallel shafts. The gear pairs are placed in separate gear boxes, which also contain the supporting ball bearings. One of the shafts consists of two sections connected by a coupling. Loading is accomplished by locking one side of the coupling and applying torque to the other. The conditions of the test were:
Speed r.p.m 3200 Oil temperature C Oil flow-rate cc./scc 10 Load in increments 5 min. at each setting.
Results of the evaluations are given in Table I and for the purpose of comparison, the results obtained from the use o f ihe base oil alone and with other known extreme pressure compositions are also given.
Table I Composition: Score load, lbs/in. A through I 5,600 1010 mineral oil+2% C alkenyl succinic acid 1,400 1010 mineral oil +2% malonic acid 2,800 1010 mineral oil+2% 3-hexadecyl adipic acid 1,400 1010 mineral oil+2% dodecylmercapto succinic acid 1,400 1010 mineral oil+10% glycerol monooleate 1,800 1010 mineral oil+2% C13H27OH (Oxo process) 1010 mineral oil The following compositions were also tested for stability in the Dornt Oxidation Test described in the Natural Petroleum News, September 17, 1941, pages 294-6 under the following conditions: 302 F., iron catalyst, mineral white oil base and additive amount in each example was about 1% by weight and the results are shown in Table II.
The mercaptomethylphosphono compounds of this invention are useful also for providing superior load-carrying properties for lubricating oils which contain minor amounts of other agents, such as silicone anti-foaming agents, alkylphenol anti-oxidants, polyacrylate ester viscosity-index improvers, long chain fatty acids such as lauric and oleic acids, oiliness agents and the like.
I claim as my invention:
1. As a compound a C alkyl mercaptomethylphosphonic acid.
2. As a compound, decyl mercaptomethylphosphonic acid.
References Cited by the Examiner UNITED STATES PATENTS OTHER REFERENCES Arbuzov et al.; J. Gen. Chem. U.S.S.R. (English 0 translation), vol. 27, pp. 2419-2421 (1957).
CHARLES B. PARKER, Primary Examiner.

Claims (1)

1. AS A COMPOUND A C10-18 ALKYL MERCAPTOMETHYLPHOSPHONIC ACID.
US305809A1959-04-131963-08-30Alkyl mercaptomethylphosphonic acidsExpired - LifetimeUS3198826A (en)

Priority Applications (19)

Application NumberPriority DateFiling DateTitle
BE611851DBE611851A (en)1959-04-13
BE626579DBE626579A (en)1959-04-13
NL250415DNL250415A (en)1959-04-13
NL272803DNL272803A (en)1959-04-13
NL272804DNL272804A (en)1959-04-13
NL109943DNL109943C (en)1959-04-13
NL287245DNL287245A (en)1959-04-13
FR824022AFR1253771A (en)1959-04-131960-04-11 Hydrocarbylmercaptomethylphosphono compounds and compositions containing them
DES68011ADE1151085B (en)1959-04-131960-04-11 Lubricant mixture
GB12814/60AGB904968A (en)1959-04-131960-04-11Mercaptomethyl phosphono compounds and compositions containing them
FR882715AFR81706E (en)1959-04-131961-12-21 Hydrocarbylmercaptomethylphosphono compounds and compositions containing them
GB45905/61AGB955357A (en)1959-04-131961-12-21Organophosphorus-substituted dimethyl disulphides, and lubricant and fuel compositions containing the same
FR882716AFR81903E (en)1959-04-131961-12-21 Hydrocarbylmercaptomethyl-phosphono compounds and compositions containing them
GB45909/61AGB1010536A (en)1959-04-131961-12-21Organic phosphonic compounds useful as fuel and lubricant additives, and compositions containing organic phosphonic compounds
GB48702/62AGB957772A (en)1959-04-131962-12-27Polythiahydrocarbylphosphono compounds and compositions containing them
FR919847AFR83758E (en)1959-04-131962-12-27 Hydrocarbylmercaptomethyl-phosphono compounds and compositions containing them
US305809AUS3198826A (en)1959-04-131963-08-30Alkyl mercaptomethylphosphonic acids
US312329AUS3316332A (en)1959-04-131963-09-30Sulfoxy alkyl phosphono compounds
US472663AUS3309428A (en)1959-04-131965-07-16Oil-soluble bis(methylphosphonodisulfides

Applications Claiming Priority (8)

Application NumberPriority DateFiling DateTitle
US805686AUS3112271A (en)1959-04-131959-04-13Liquid hydrocarbon composition
US77817AUS3238131A (en)1960-12-231960-12-23Lubricating compositions containing bis(phosphono-methyl) disulfides
US77830AUS3112269A (en)1960-12-231960-12-23Lubricating compositions containing sulfoxy alkyl phosphono compounds
US162924AUS3226322A (en)1961-12-281961-12-28Liquid hydrocarbon composition and additives therefor
US183036AUS3232882A (en)1962-03-281962-03-28Lubricating oil compositions
US305809AUS3198826A (en)1959-04-131963-08-30Alkyl mercaptomethylphosphonic acids
US312329AUS3316332A (en)1959-04-131963-09-30Sulfoxy alkyl phosphono compounds
US472663AUS3309428A (en)1959-04-131965-07-16Oil-soluble bis(methylphosphonodisulfides

Publications (1)

Publication NumberPublication Date
US3198826Atrue US3198826A (en)1965-08-03

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ID=27574562

Family Applications (3)

Application NumberTitlePriority DateFiling Date
US305809AExpired - LifetimeUS3198826A (en)1959-04-131963-08-30Alkyl mercaptomethylphosphonic acids
US312329AExpired - LifetimeUS3316332A (en)1959-04-131963-09-30Sulfoxy alkyl phosphono compounds
US472663AExpired - LifetimeUS3309428A (en)1959-04-131965-07-16Oil-soluble bis(methylphosphonodisulfides

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Application NumberTitlePriority DateFiling Date
US312329AExpired - LifetimeUS3316332A (en)1959-04-131963-09-30Sulfoxy alkyl phosphono compounds
US472663AExpired - LifetimeUS3309428A (en)1959-04-131965-07-16Oil-soluble bis(methylphosphonodisulfides

Country Status (5)

CountryLink
US (3)US3198826A (en)
BE (2)BE626579A (en)
DE (1)DE1151085B (en)
GB (4)GB904968A (en)
NL (5)NL250415A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3957858A (en)*1970-04-131976-05-18Monsanto CompanySubstituted ethane diphosphonic acids and salts and esters thereof

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
GB1357745A (en)*1971-05-051974-06-26Exxon Research Engineering CoLubricating oil compositions
US4082793A (en)*1977-02-091978-04-04The United States Of America As Represented By The Secretary Of The NavyAromatic phosphinic acids containing sulfone linkage
US4317795A (en)*1979-04-051982-03-02Phillips Petroleum CompanyCatalytic alkylation of hydrocarbons
FR2631039A1 (en)*1988-05-061989-11-10Elf France
USD334976S (en)1991-08-231993-04-20John Manufacturing LimitedMini fan
US5443744A (en)*1993-12-171995-08-22Exxon Chemical Patent Inc.Non silicone aggresive alkyl phosphates as lubrication oil additives

Citations (3)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US2535174A (en)*1949-04-071950-12-26Us Rubber CoMercaptoethanephosphonates
US2793225A (en)*1955-08-191957-05-21Union Oil CoProcess for preparing phosphonic acid esters
US2963505A (en)*1954-11-061960-12-06Bayer AgSulphoxides-containing esters of the phosphoric and thiophosphoric acids

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US2708204A (en)*1950-08-111955-05-10Shell DevHalogen- and phosphorus-containing compounds
DE935547C (en)*1952-12-091955-11-24Henkel & Cie Gmbh Process for the production of condensation products with organically bound phosphorus
US2857304A (en)*1954-11-231958-10-21Monsanto ChemicalsDithiodimethylene diphosphonates

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US2535174A (en)*1949-04-071950-12-26Us Rubber CoMercaptoethanephosphonates
US2963505A (en)*1954-11-061960-12-06Bayer AgSulphoxides-containing esters of the phosphoric and thiophosphoric acids
US2793225A (en)*1955-08-191957-05-21Union Oil CoProcess for preparing phosphonic acid esters

Cited By (1)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3957858A (en)*1970-04-131976-05-18Monsanto CompanySubstituted ethane diphosphonic acids and salts and esters thereof

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Publication numberPublication date
DE1151085B (en)1963-07-04
BE611851A (en)
NL272803A (en)
US3316332A (en)1967-04-25
NL250415A (en)
GB904968A (en)1962-09-05
NL109943C (en)
GB1010536A (en)1965-11-17
NL287245A (en)
GB955357A (en)1964-04-15
US3309428A (en)1967-03-14
NL272804A (en)
GB957772A (en)1964-05-13
BE626579A (en)

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