US5136101A
Expired / Lapsed
US
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Process for the preparation of ketones
Assignee: Shell USA Inc
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Filing: 1991-09-30
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Granted: 1992-08-04
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Expires: 2011-09-30
Abstract
Abstract A process for the preparation of a ketone which comprises reacting the corresponding secondary alkanol with a solubilized stable free radical nitroxide having the formula: ##STR1## wherein each of R 1 , R 2 , R 3 and R 4 is an alkyl, aryl or heteroatom substituted alkyl group having 1 to about 15 carbon atoms and each of R 5 and R 6 is alkyl, hydrogen, aryl or a substituted heteroatom, and an alkali metal nitrosodisulfonate in the presence of an oxidant at a temperature in the range of from about -10° C. to about 80° C. and thereafter separating out the ketone.
Inventors
- 👤 Herbert E. Fried
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-25 16:43
CPC Classifications
C; C07; C07C; C07C45/00; C07C45/27; C07C45/29
Claims Analysis
Total Claims: 19
Claim 1
Independent Claim
104 words
A process for the preparation of a ketone which comprises reacting the corresponding secondary alkanol with a solubilized stable free radical nitroxide having the formula: ##STR5## wherein each of R 1 , R 2 , R 3 and R 4 is an alkyl, aryl or heteroatom substituted alkyl group having 1 to about 15 carbon atoms and each of R 5 and R 6 is alkyl, hydrogen, aryl or a substituted heteroatom, and an alkali metal nitrosodisulfonate in the presence of an oxidant at a temperature in the range of from about -10° C. to about 80° C. and thereafter separating out the ketone.
Claim 2
Dependent Claim
104 words
A process for the preparation of a ketone which comprises reacting the corresponding secondary alkanol with a solubilized stable free radical nitroxide having the formula: ##STR5## wherein each of R 1 , R 2 , R 3 and R 4 is an alkyl, aryl or heteroatom substituted alkyl group having 1 to about 15 carbon atoms and each of R 5 and R 6 is alkyl, hydrogen, aryl or a substituted heteroatom, and an alkali metal nitrosodisulfonate in the presence of an oxidant at a temperature in the range of from about -10° C. to about 80° C. and thereafter separating out the ketone.
Claim 3
Dependent Claim
27 words
The process of claim 1 wherein the solubilized stable free radical nitroxide is selected from the group consisting of 2,2,6,6-tetramethyl-piperidine-1-oxyl, 4-hydroxy-2,2,6,6-tetramethyl-piperidine-1-oxyl, 4-oxo-2,2,6,6-tetramethyl-piperidine-1-oxyl, 2,2,6,6-tetramethyl-piperidine-1-oxyl-4-sulfate, 4-alkoxy-2,2,6,6-tetramethyl-piperidine-1-oxyl and mixtures thereof.
Claim 4
Dependent Claim
25 words
The process of claim 2 wherein the solubilized stable free radical nitroxide is selected from the group consisting of 2,2,6,6-tetramethyl-piperidine-1-oxyl, 2,2,6,6-tetramethyl-piperidine-1-oxyl-4-sulfate, 4-alkoxy-2,2,6,6-tetramethyl-piperidine-1-oxyl and mixtures thereof.
Claim 5
Dependent Claim
36 words
The process of claim 1 wherein the stable free radical nitroxide is dissolved in a solvent selected from the group consisting of acetonitrile, tertiary butyl alcohol, tertiary amyl alcohol, ethyl acetate, sulfolane, dichloromethane and mixtures thereof.
Claim 6
Dependent Claim
29 words
The process of claim 4 wherein the stable free radical nitroxide is dissolved in a solvent selected from the group consisting of tertiary butyl alcohol, acetonitrile and mixtures thereof.
Claim 7
Dependent Claim
24 words
The process of claim 1 wherein said alkali metal nitrosodisulfonate is selected from the group consisting of potassium nitrosodisulfonate, sodium nitrosodisulfonate, and mixtures thereof.
Claim 8
Dependent Claim
13 words
The process of claim 6 wherein said alkali metal nitrosodisulfonate is potassium nitrosodisulfonate.
Claim 9
Dependent Claim
31 words
The process of claim 1 wherein said secondary alkanol is contacted with said solubilized stable free radical nitroxide and said alkali metal nitrosodisulfonate, followed by the addition thereto of said oxidant.
Claim 10
Dependent Claim
38 words
The process of claim 8 wherein the amount of solubilized stable free radical nitroxide is in the range of from about 1 mole percent to about 50 mole percent, basis the number of moles of said secondary alkanol.
Claim 11
Dependent Claim
36 words
The process of claim 8 wherein the amount of said alkali metal nitrosodisulfonate is in the range of from 1 mole percent to about 35 mole percent, basis the number of moles of said secondary alkanol.
Claim 12
Dependent Claim
30 words
The process of claim 1 wherein said secondary alkanol is contacted with said alkali metal nitrosodisulfonate and said oxidant, followed by the addition thereto of said stable free radical nitroxide.
Claim 13
Dependent Claim
38 words
The process of claim 11 wherein the amount of solubilized stable free radical nitroxide is in the range of from about 1 mole percent to about 50 mole percent, basis the number of moles of said secondary alkanol.
Claim 14
Dependent Claim
36 words
The process of claim 11 wherein the amount of said alkali metal nitrosodisulfonate is in the range of from 1 mole percent to about 35 mole percent, basis the number of moles of said secondary alkanol.
Claim 15
Dependent Claim
12 words
The process of claim 1 wherein said oxidant is an oxygen-containing gas.
Claim 16
Dependent Claim
21 words
The process of claim 14 wherein said oxygen containing gas is selected from the group consisting of pure oxygen and air.
Claim 17
Dependent Claim
12 words
The process of claim 15 wherein said oxygen-containing gas is pure oxygen.
Claim 18
Dependent Claim
30 words
The process of claim 1 wherein said process is carried out at a temperature in the range of from about 25° C. to about 50° C. and at atmospheric pressure.
Claim 19
Dependent Claim
30 words
The process of claim 17 wherein said process is carried out at a temperature in the range of from about 30° C. to about 40° C. and at atmospheric pressure.
References Cited (Backward Citations)
US4620033A
Cited
JPH0596516A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1995-08-04 | 1996-02-03 | 1996-08-04 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1999-08-04 | 2000-02-03 | 2000-08-04 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2003-08-04 | 2004-02-03 | 2004-08-04 | $7700.00 | Window Closed / Lapsed |