GB274894A - Manufacture of carboxylic acids of acenaphthene - Google Patents
Manufacture of carboxylic acids of acenaphtheneInfo
- Publication number
- GB274894A GB274894A GB19492/27A GB1949227A GB274894A GB 274894 A GB274894 A GB 274894A GB 19492/27 A GB19492/27 A GB 19492/27A GB 1949227 A GB1949227 A GB 1949227A GB 274894 A GB274894 A GB 274894A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acenaphthene
- carboxylic acids
- acetylacenaphthene
- chloracetyl
- chloroform
- 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
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/29—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with halogen-containing compounds which may be formed in situ
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
274,894. I. G. Farbenindustrie Akt.- Ges. July 24, 1926, [Convention date]. Acenaphthene carboxylic acids: chloroform. - Acenaphthene carboxylic acids are obtained by treating acetyl-, diacetyl-, chloracetyl-, or di(chloracetyl)-acenaphthene or a substitution product of any of them with an alkaline hypochlorite solution, chloroform being eliminated. In an example, 5-chloracetylacenaphthene or 5- acetylacenaphthene is heated with an excess of alkaline hypochlorite solution, and, on cooling, the sodium salt of 5-acenaphthenecarboxylic acid separates. An acenaphthenedicarboxylic acid is obtained from the di(chloracetyl)acenaphthene produced from acenaphthene and 2 molecular proportions of chloracetylchloride, or by condensation of 5-chloracetylacenaphthene with chloracetylchloride. In the same way, 5-bromo-6- acenaphthenecarboxylic acid may be prepared from 5-bromo-6-acetylacenaphthene, obtained by bromination of acetylacenaphthene in presence of chloroform.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE274894X | 1926-07-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB274894A true GB274894A (en) | 1928-02-16 |
Family
ID=6022790
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19492/27A Expired GB274894A (en) | 1926-07-24 | 1927-07-22 | Manufacture of carboxylic acids of acenaphthene |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB274894A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2884448A (en) * | 1956-07-02 | 1959-04-28 | Gen Aniline & Film Corp | Hydrolysis of n-substituted amides |
-
1927
- 1927-07-22 GB GB19492/27A patent/GB274894A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2884448A (en) * | 1956-07-02 | 1959-04-28 | Gen Aniline & Film Corp | Hydrolysis of n-substituted amides |
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