GB353373A - Process for the manufacture of hydroaromatic carboxylic acids - Google Patents
Process for the manufacture of hydroaromatic carboxylic acidsInfo
- Publication number
- GB353373A GB353373A GB842/31A GB84231A GB353373A GB 353373 A GB353373 A GB 353373A GB 842/31 A GB842/31 A GB 842/31A GB 84231 A GB84231 A GB 84231A GB 353373 A GB353373 A GB 353373A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- carboxylic acids
- salt
- hydroaromatic
- perhydronaphthyl
- 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
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/36—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by hydrogenation of carbon-to-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Hydroaromatic carboxylic acids are obtained by the catalytic hydrogenation of a salt, preferably an alkali salt, of an aromatic carboxylic acid or substitution product thereof in aqueous solution. A nickel catalyst is used. As examples are mentioned the conversion of (1) phthalic acid to trans-hexahydrophthalic acid, (2) naphthalic acid to tetra-hydronaphthalic acid, (3) naphthoyl benzoic acid to a mixture of perhydronaphthyl methyl cyclohexane carboxylic acids. The sodium salts are used as the initial material in each case.ALSO:Hydroaromatic carboxylic acids are obtained by the catalytic hydrogenation of a salt, preferably an alkali salt, of an aromatic carboxylic acid or substitution product thereof in aqueous solution. A nickel catalyst is used. Examples referred to are the conversion of (1) phthalic acid to transhexahydrophthalic acid, (2) naphthalic acid to tetrahydronaphthalic acid, (3) naphthoyl benzoic acid to a mixture of perhydronaphthyl methyl cyclohexane carboxylic acids. The sodium salts are used as the initial material in each case.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE353373X | 1930-01-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB353373A true GB353373A (en) | 1931-07-23 |
Family
ID=6281590
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB842/31A Expired GB353373A (en) | 1930-01-11 | 1931-01-09 | Process for the manufacture of hydroaromatic carboxylic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB353373A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6541662B2 (en) * | 2000-12-26 | 2003-04-01 | Mitsubishi Gas Chemical Company, Inc. | Process for producing a hydrogenation product of an aromatic carboxylic acid |
-
1931
- 1931-01-09 GB GB842/31A patent/GB353373A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6541662B2 (en) * | 2000-12-26 | 2003-04-01 | Mitsubishi Gas Chemical Company, Inc. | Process for producing a hydrogenation product of an aromatic carboxylic acid |
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