GB940381A - Preparation of dialkyl sulphoxides - Google Patents
Preparation of dialkyl sulphoxidesInfo
- Publication number
- GB940381A GB940381A GB21007/60A GB2100760A GB940381A GB 940381 A GB940381 A GB 940381A GB 21007/60 A GB21007/60 A GB 21007/60A GB 2100760 A GB2100760 A GB 2100760A GB 940381 A GB940381 A GB 940381A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphoxides
- tri
- dialkyl
- octyl
- sulphoxide
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
Abstract
Dialkyl sulphoxides are prepared by mixing a solution of an alkyl aluminium compound in an inert organic solvent with a solution of thionyl chloride in an inert organic solvent under an atmosphere of an inert gas while maintaining throughout the addition a temperature of from -25 DEG to 100 DEG C. and then maintaining the mixture at a temperature of from 0 DEG C. to 100 DEG C. until the thionyl chloride and alkyl aluminium compound have reacted, hydrolyzing the reaction mixture with simultaneous or subsequent cooling to maintain it below 100 DEG C. and then recovering the dialkyl sulphoxide. The alkyl aluminium reactant may be a compound having the general formula R3Al, R2Al OR or R2Al Cl wherein R is an alkyl group. The solvents may be hydrocarbons or ethers. The mixing is preferably effected at 0 DEG -30 DEG C. and the mixture is thereafter preferably maintained at 30 DEG -80 DEG C. In examples: (1) di-n-octyl sulphoxide is prepared from tri-n-octyl aluminium; triethyl, tri propyl, tri butyl and tri dodecyl aluminiums may also be used to form the corresponding dialkyl sulphoxides; (2) dihexyl sulphoxide is prepared from dihexyl aluminium hexoxide or chloride. The sulphoxides may be used as oxidation inhibitors in lubricating oils or in diesel fuel to raise the cetane number.ALSO:Diesel fuels comprise dialkyl sulphoxides as cetane number improvers. Specified sulphoxides are di-ethyl, -propyl, -butyl, -hexyl, -n-octyl and dodecyl sulphoxides.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US834959A US2947787A (en) | 1959-08-20 | 1959-08-20 | Preparation of dialkyl sulfoxides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB940381A true GB940381A (en) | 1963-10-30 |
Family
ID=25268215
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB21007/60A Expired GB940381A (en) | 1959-08-20 | 1960-06-15 | Preparation of dialkyl sulphoxides |
Country Status (3)
Country | Link |
---|---|
US (1) | US2947787A (en) |
BE (1) | BE592357A (en) |
GB (1) | GB940381A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3546117A (en) * | 1965-06-03 | 1970-12-08 | Chevron Res | Thio compounds as additives in fluids used in engines |
US3413354A (en) * | 1966-01-04 | 1968-11-26 | Chevron Res | Method of preparing aryl sulfoxides |
GB1062405A (en) * | 1966-04-18 | 1967-03-22 | Akad Wissenschaften Ddr | Process for the preparation of aryl sulphoxides |
US4122021A (en) * | 1977-05-16 | 1978-10-24 | Uniroyal, Inc. | Antioxidant stabilized lubricating oils |
US4469586A (en) * | 1982-09-30 | 1984-09-04 | Chevron Research Company | Heat exchanger antifoulant |
WO2016114307A1 (en) * | 2015-01-16 | 2016-07-21 | 凸版印刷株式会社 | Transdermal-administration-device accommodating body |
-
1959
- 1959-08-20 US US834959A patent/US2947787A/en not_active Expired - Lifetime
-
1960
- 1960-06-15 GB GB21007/60A patent/GB940381A/en not_active Expired
- 1960-06-28 BE BE592357A patent/BE592357A/en unknown
Also Published As
Publication number | Publication date |
---|---|
BE592357A (en) | 1960-10-17 |
US2947787A (en) | 1960-08-02 |
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