GB1089473A - Preparation of acetoacetarylamides - Google Patents
Preparation of acetoacetarylamidesInfo
- Publication number
- GB1089473A GB1089473A GB42713/65A GB4271365A GB1089473A GB 1089473 A GB1089473 A GB 1089473A GB 42713/65 A GB42713/65 A GB 42713/65A GB 4271365 A GB4271365 A GB 4271365A GB 1089473 A GB1089473 A GB 1089473A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acetoacet
- acetoacetarylamides
- preparation
- reaction
- per
- 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
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/02—Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/10—Preparation of carboxylic acid amides from compounds not provided for in groups C07C231/02 - C07C231/08
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Acetoacetarylamides are prepared by adding to a reaction zone, at a rate sufficiently slow to avoid substantial build-up of reactants, stoichiometric proportions of arylamine or arylenediamine and diketene, the reaction being conducted at 0-50 DEG C. in presence of 1-10 parts water (by wt.) per parts of total reactants, while agitating with a force of at least 0.5 h.p. per 100 gallons of reaction medium. Examples describe the preparation of acetoacetanilide, acetoacet - o - toluidide, acetoacet - o - chloroanilide, acetoacet-o-anisidide and the bis-acetoacetyl derivatives of 2,4-tolyenediamine and m-phenylenediamine, from the corresponding amines, but a number of other suitable amines are also listed.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB42713/65A GB1089473A (en) | 1965-10-08 | 1965-10-08 | Preparation of acetoacetarylamides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB42713/65A GB1089473A (en) | 1965-10-08 | 1965-10-08 | Preparation of acetoacetarylamides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1089473A true GB1089473A (en) | 1967-11-01 |
Family
ID=10425643
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB42713/65A Expired GB1089473A (en) | 1965-10-08 | 1965-10-08 | Preparation of acetoacetarylamides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1089473A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105418422A (en) * | 2015-12-21 | 2016-03-23 | 常熟市柏伦精细化工有限公司 | Preparation technology of novel naphthol AS-IRG (2,5-Dimethoxy-4-chloroacetoacetanilide) |
-
1965
- 1965-10-08 GB GB42713/65A patent/GB1089473A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105418422A (en) * | 2015-12-21 | 2016-03-23 | 常熟市柏伦精细化工有限公司 | Preparation technology of novel naphthol AS-IRG (2,5-Dimethoxy-4-chloroacetoacetanilide) |
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