反应详情
EQUATION
反应方程式
REACTANTS
反应物
Carbon dioxide
CO2
Hydrogen peroxide
H2O2
Hydroxylamine
H3NO
Benzoic acid, 4-chloro-3-nitro-
C7H4ClNO4
Benzenethiol
C6H6S
3-Methylbutyl nitrite
C5H11NO2
Sodium Hydroxide
HNaO
2 次
4-Chlorobenzothiazol-2-ylamine
C7H5ClN2S
Ethanedioyl dichloride
C2Cl2O2
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The benzisoxazole-, benzisoxazole-, and benzothiazolecarboxylic acids were prepared using similar strategies outlined for the indazole acids. For example, ethyl 6-bromobenzisoxazole-3-carboxylate was prepared from 2,5-dibromonitrobenzene by reaction with diethyl malonate, saponification and decarboxylation, and reaction with isoamylnitrite. Ethyl benzisoxazole-3-carboxylate was obtained by hydrogenolysis of the 6-bromo derivative. 4-Benzothiazolecarboxylic acid was prepared from 2-amino-4-chloro-benzothiazole by reaction with isoamyl nitrite followed by metal-halogen exchange and trapping with carbon dioxide. 5-Benzothiazolecarboxylic acid was prepared from 4-chloro-3-nitrobenzoic acid by reaction with Na2S and sodium hydroxide followed by reduction with zinc in formic acid. 3-Benzisothiazolecarboxylic acid was prepared from thiophenol by reaction with oxalyl chloride and aluminum chloride followed by treatment with hydroxylamine, hydrogen peroxide, and sodium hydroxide.