돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4702생성일: 2026년 10월 23일

Benzo(d)thiazol-2-amine → 1-(1,3-Benzothiazol-2-yl)propan-2-one

https://huagongshe.com/ko/reaction/4702

반응식

참여 물질

역할이름HCID투입량
반응물Benzo(d)thiazol-2-amineHCID 8706—
반응물Sodium HydroxideHCID 14798—
반응물SodiumHCID 5360545—
반응물PotassiumHCID 5462222—
반응물N-(2-Sulfanylphenyl)ureaHCID 23358470—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매DiketeneHCID 12661—
생성물1-(1,3-Benzothiazol-2-yl)propan-2-oneHCID 32029479.4%

반응 단계

The water-moist 2-mercaptophenylurea obtained according to European Pat. No. 0,039,483, Example 1, paragraph 1, by reacting 150 parts of 2-aminobenzothiazole with 150 parts of sodium hydroxide and working up the mixture with water, or an appropriate amount of the sodium or potassium salt of the said 2-mercaptophenylurea, is dissolved in 500 parts of 50% strength acetic acid, and 118 parts of diketene are then added dropwise in the course of 2 hours at 45° to 50° C. Stirring is continued for 1 hour, after which the mixture is heated to the reflux temperature and kept at a temperature of 95° C.-100° C. for 2 hours. It is then cooled to room temperature, and the precipitated 2-acetonylbenzothiazole of the formula ##STR13## is isolated by filtration and dried in vacuo at 60° C.-80° C. 151.7 parts of a product of melting point 118° C.-119° C. are obtained; this corresponds to a yield of 79.4%, based on 2-aminobenzothiazole employed.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727154
출처 데이터셋uspto-grants-1988_02
ORD IDord-3f4e5fd49dba41ce9980468ba16d9ddd
출처 메모uspto-grants-1988_02