돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 580604생성일: 2026년 10월 24일

Water → 4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholide

https://huagongshe.com/ko/reaction/580604

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물Phosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl esterHCID 11207805—
반응물HCID 13373314HCID 13373314—
용매TetrahydrofuranHCID 8028—
생성물4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholideHCID 54521919—

반응 단계

A solution of 5.3 g (0.02 mol) of diethylphosphonoacetic acid morpholide in 100 ml of dry tetrahydrofuran was slowly added dropwise, while stirring, to a suspension of 1 g of sodium hydride (0.02 mol, 50% in oil) in 50 ml of dry tetrahydrofuran. Slight heating and strong foaming occurred. After all had been added, the mixture was stirred for 10 minutes more. A solution of 3 g (0.01 mol) of 4-amino-3,4',5-trichlorobenzophenone in 20 ml of dry tetrahydrofuran was added dropwise to the resulting clear solution, and the mixture was heated for 16 hours at reflux temperature. After cooling, the solution was poured into water, and the aqueous mixture was extracted exhaustively with methylene chloride. The methylene chloride phase was dried with sodium sulfate and evaporated by evaporation in vacuo. The residue was crystallized from isopropanol/petroleum ether. The colorless crystals thus obtained, melting point 150°-155° C., contained the cis/trans isomers in a ratio of 1:3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04753934
출처 데이터셋uspto-grants-1988_06
ORD IDord-d3a7eb78bd444d0fb967eeb28ced0d84
출처 메모uspto-grants-1988_06