GB661746A - Improvements in or relating to the production of barbituric acids - Google Patents
Improvements in or relating to the production of barbituric acidsInfo
- Publication number
- GB661746A GB661746A GB31540/49A GB3154049A GB661746A GB 661746 A GB661746 A GB 661746A GB 31540/49 A GB31540/49 A GB 31540/49A GB 3154049 A GB3154049 A GB 3154049A GB 661746 A GB661746 A GB 661746A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethyl
- metabromphenyl
- metabromphenylacetate
- relating
- production
- 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
- C07C253/00—Preparation of carboxylic acid nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/14—Preparation of carboxylic acid nitriles by reaction of cyanides with halogen-containing compounds with replacement of halogen atoms by cyano groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
5-metabromphenyl-5-ethyl barbituric acid is obtained by converting metabromobenzyl chloride into the cyanide with potassium cyanide, saponifying and esterifying with ethyl alcohol, condensing with ethyl oxalate, eliminating carbon monoxide from the product, ethylating with ethyl halide and finally condensing the ethyl metabromphenyl-ethyl-malonate obtained with urea in methyl alcohol. The details of the reactions are given in an example. Intermediate products obtained as described above are ethyl metabromphenylacetate, sodium ethyl oxalyl - metabromphenylacetate and sodium ethyl metabromphenyl-malonate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR661746X | 1948-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB661746A true GB661746A (en) | 1951-11-28 |
Family
ID=9011066
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31540/49A Expired GB661746A (en) | 1948-12-20 | 1949-12-08 | Improvements in or relating to the production of barbituric acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB661746A (en) |
-
1949
- 1949-12-08 GB GB31540/49A patent/GB661746A/en not_active Expired
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