GB359865A - Process for the manufacture of disubstituted carbamic acid esters - Google Patents
Process for the manufacture of disubstituted carbamic acid estersInfo
- Publication number
- GB359865A GB359865A GB9576/31A GB957631A GB359865A GB 359865 A GB359865 A GB 359865A GB 9576/31 A GB9576/31 A GB 9576/31A GB 957631 A GB957631 A GB 957631A GB 359865 A GB359865 A GB 359865A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbamic acid
- acid esters
- dimethylaminophenol
- aliphatic
- nitrogen atom
- 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
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Disubstituted carbamic acid esters of aromatic hydroxy compounds containing a tertiary nitrogen atom in aliphatic or heterocyclic combination are prepared by (1) interaction of dialkyl-, arylalkyl-or diaryl-carbamic acid halides with the alkali salts of aromatic hydroxy compounds containing a tertiary nitrogen atom in aliphatic or heterocyclic combination, or (2) treating the carbamic acid esters of aromatic hydroxy compounds containing a tertiary nitrogen atom in aliphatic or heterocyclic combination with dialkyl-, arylalkyl- or diaryl-amines or piperidine. The products possess similar properties to physostigmine. Examples are given of the preparation of (1) the methylphenyl- and diphenyl-carbamic acid esters of m-dimethyl-aminophenol from methylphenyl- and diphenyl-carbamic acid chlorides respectively and m-dimethylaminophenol; in the same way, the dimethylcarbamic acid esters of o-oxybenzyldiethylamine, 8-hydroxyquinoline and m-dimethylaminophenol are obtained; (3) the pentamethylene-carbamic acid ester of m-dimethylaminophenol from tetramethyl-m-m-diaminophenylcarbonic acid ester and piperidine. Specification 342,237 is referred to. o-Oxybenzyldiethylamine is prepared from phenol, formaldehyde and diethylamine.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE359865X | 1931-01-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB359865A true GB359865A (en) | 1931-10-29 |
Family
ID=6291312
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9576/31A Expired GB359865A (en) | 1931-01-02 | 1931-03-30 | Process for the manufacture of disubstituted carbamic acid esters |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB359865A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2524185A (en) * | 1948-10-01 | 1950-10-03 | Merck E | Thymyl n-isoamylcarbamate |
-
1931
- 1931-03-30 GB GB9576/31A patent/GB359865A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2524185A (en) * | 1948-10-01 | 1950-10-03 | Merck E | Thymyl n-isoamylcarbamate |
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