US4034006A
Expired / Lapsed
US
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Process for the manufacture of alkali salts of 3,5-disubstituted 4-hydroxybenzoic acids and their free acids
Assignee: Novartis Corp
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Filing: 1975-02-24
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Granted: 1977-07-05
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Expires: 1995-02-24
Abstract
Abstract A new process for the preparation of alkalimetal salts of 3,5-substituted 4-hydroxybenzoic acids and the free acids thereof, which comprises reacting a 2,6-disubstituted phenol in a mixture of water and a dipolar aprotic solvent with an alkalimetal hydroxide, removing the water, treating the reaction mixture with carbon dioxide and in case of preparing the free acids treating the reaction mixture with a mineral acid. The alkalimetal salts of 4-hydroxybenzoic acids and the free acids thereof are compounds which can be used as intermediates for stabilizers.
Inventors
- 👤 Hanns Lind
- 👤 Jean Rody
- 👤 Heimo Brunnetti
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-30 11:25
CPC Classifications
C; C07; C07C; C07C51/00; C07C51/15; C07C65/00; C07C65/01; C07C65/03
Claims Analysis
Total Claims: 7
Claim 1
Independent Claim
136 words
A process for the manufacture of compounds of the general formula I ##STR3## wherein R 1 and R 2 are both tert.-butyl, sec.-butyl or cycloocytl, or R 1 is tert.-butyl and R 2 is methyl or R 1 is tert.-butyl and R 2 is cyclohexyl, and M is hydrogen or an alkali metal atom, in which process a phenol of the general formula II ##STR4## wherein R 1 and R 2 have the meaning indicated under the formula I, is treated, in a mixture of water and a dipolar aprotic solvent, with an alkali metal hydroxide and the reaction product, after removal of the water, is reacted, without intermediate isolation and in the organic medium, at elevated temperature, with carbon dioxide under normal pressure and the acid is optionally liberated from the resulting alkali metal salt.
Claim 2
Dependent Claim
136 words
A process for the manufacture of compounds of the general formula I ##STR3## wherein R 1 and R 2 are both tert.-butyl, sec.-butyl or cycloocytl, or R 1 is tert.-butyl and R 2 is methyl or R 1 is tert.-butyl and R 2 is cyclohexyl, and M is hydrogen or an alkali metal atom, in which process a phenol of the general formula II ##STR4## wherein R 1 and R 2 have the meaning indicated under the formula I, is treated, in a mixture of water and a dipolar aprotic solvent, with an alkali metal hydroxide and the reaction product, after removal of the water, is reacted, without intermediate isolation and in the organic medium, at elevated temperature, with carbon dioxide under normal pressure and the acid is optionally liberated from the resulting alkali metal salt.
Claim 3
Dependent Claim
10 words
A process according to claim 1 wherein M is hydrogen.
Claim 4
Dependent Claim
27 words
A process according to claim 1 wherein the starting material is a phenol of the general formula II in which R 1 and R 2 are tert.-butyl.
Claim 5
Dependent Claim
26 words
A process according to claim 1 wherein the mixture of water and a dipolar aprotic solvent which is used is a mixture of water and diemthylformamide.
Claim 6
Dependent Claim
20 words
A process according to claim 1 wherein the reaction is carried out at a temperature of 60° to 85° C.
Claim 7
Dependent Claim
15 words
A process according to claim 1 wherein the alkali metal hydroxide used is sodium hydroxide.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1980-07-04 | 1981-01-03 | 1981-07-05 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1984-07-04 | 1985-01-03 | 1985-07-05 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1988-07-04 | 1989-01-03 | 1989-07-05 | $7700.00 | Window Closed / Lapsed |