돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27423생성일: 2026년 10월 24일

Water → 2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepine

https://huagongshe.com/ko/reaction/27423

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl (4-chlorophenyl)acetateHCID 84177—
반응물SodiumHCID 5360545—
반응물HCID 178483040HCID 178483040—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
생성물2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepineHCID 53941548—

반응 단계

Add (drop by drop at 90° in a stream of nitrogen to let the alcohol escape) a solution of 4.6 g of sodium in 100 ml of ethyl alcohol to a mixture of 53.2 g of the title compound of Example 1 and 29.8 g of ethyl 4-chlorophenylacetate. Stir it for a further 4 hours at 90° and then cool it to ambient temperature. Mix the cooled reaction mixture with 100 ml of water and 100 ml of diethyl ether, collect the organic phase and dry the latter over sodium sulfate. Concentrate the dried organic phase and then distil off any excess ethyl 4-chlorophenylacetate under a high vacuum to obtain a crude yield [15.5 g (34% of theory)] of the title compound as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04221788
출처 데이터셋uspto-grants-1980_09
ORD IDord-ca593dee24784df38759aae09bcc0859
출처 메모uspto-grants-1980_09