US4059636A
Expired / Lapsed
US
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Mercaptans by catalytic cleavage of organic sulfides
Assignee: Phillips Petroleum Co
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Filing: 1976-05-04
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Granted: 1977-11-22
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Expires: 1996-05-04
Abstract
Abstract A method is provided for preparing mercaptans by catalytic cleavage of organic sulfides with hydrogen sulfide in the presence of a supported phosphotungstic acid catalyst. The process is particularly advantageous with n-alkyl sulfide feedstock and being highly selective for producing n-alkyl mercaptan product. In one embodiment the presence of carbon disulfide in the reaction mixture increases the conversion at low temperature as compared to the process without the presence of carbon disulfide.
Inventors
- 👤 Donald H. Kubicek
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-29 20:01
CPC Classifications
C; C07; C07C; C07C319/00; C07C319/02; C07C319/06
Claims Analysis
Total Claims: 9
Claim 1
Independent Claim
37 words
A method in which mercaptans are prepared by catalytic cleavage of organic sulfides with hydrogen sulfide in the presence of a supported phosphotungstic acid catalyst at a temperature and pressure sufficient for catalytic cleavage of organic sulfides.
Claim 2
Independent Claim
37 words
A method in which mercaptans are prepared by catalytic cleavage of organic sulfides with hydrogen sulfide in the presence of a supported phosphotungstic acid catalyst at a temperature and pressure sufficient for catalytic cleavage of organic sulfides.
Claim 3
Dependent Claim
14 words
A method of claim 1 wherein carbon disulfide is present in the reaction mixture.
Claim 4
Dependent Claim
34 words
A method of claim 1 wherein the reaction is carried out at a temperature ranging from about 177° C to about 315° C and the pressure is from about 100 to about 5000 psig.
Claim 5
Dependent Claim
32 words
A method of claim 2 wherein the carbon disulfide is added to the reaction mixture in a mole ratio in the range of about 0.1/1 to about 50/1 of organic sulfide/carbon disulfide.
Claim 6
Dependent Claim
73 words
A method of claim 1 wherein the organic sulfides are represented by the formula R-S-R; wherein the R groups are independently selected from the group consisting of alkyl, cycloalkyl, aromatic, alkylaryl, arylalkyl, straight chain or branched chain with the R's being the same or different in the same molecule and with the R group selected so that the useful sulfides contain from about 2 to about 40 or more carbon atoms per molecule.
Claim 7
Dependent Claim
48 words
A method of claim 5 wherein the organic sulfide is chosen from among the group comprising dimethyl sulfide, diethyl sulfide, diisopropyl sulfide, di-n-butyl sulfide, di-n-octyl sulfide, di-n-dodecyl sulfide, di-n-eicosyl sulfide, methyl ethyl sulfide, n-pentyl-n-heptyl sulfide, dicyclohexyl sulfide, bis(4-methylcyclohexyl) sulfide, diphenyl sulfide, di-p-tolyl sulfide, bis(p-n-hexylphenyl) sulfide, and dibenzyl sulfide.
Claim 8
Dependent Claim
27 words
A method of claim 1 wherein the phosphotungstic acid catalyst is supported on a metal selected from among activated carbon, alumina, zirconia, silica, thoria, pumice, and silica-alumina.
Claim 9
Dependent Claim
10 words
A method of claim 7 wherein said material is alumina.
References Cited (Backward Citations)
US2402614A
Cited
US2829171A
Cited
US3069472A
Cited
US3214386A
Cited
US3143574A
Cited
US3231488A
Cited
US3880933A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1980-11-21 | 1981-05-23 | 1981-11-22 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1984-11-21 | 1985-05-23 | 1985-11-22 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1988-11-21 | 1989-05-23 | 1989-11-22 | $7700.00 | Window Closed / Lapsed |