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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264706생성일: 2026년 10월 25일

Sodium Hydroxide → N-{5-(4-Chlorophenyl)pent-1-en-4-yl}-N-ethoxymethyl-3,5-dimethylbenzamide

https://huagongshe.com/reaction/264706

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Chloromethyl ethyl etherHCID 18523—
반응물N-{5-(4-chlorophenyl)pent-1-en-4-yl}-3.5-dimethylbenzamideHCID 19035936—
촉매Benzyltributylammonium chlorideHCID 159952—
용매DichloromethaneHCID 6344—
생성물N-{5-(4-Chlorophenyl)pent-1-en-4-yl}-N-ethoxymethyl-3,5-dimethylbenzamideHCID 19035912—

반응 단계

2.36 ml (25.2 mmol) of chloromethyl ethyl ether are added in small portions over the course of 2 hours to a vigorously stirred solution of 5.5 g (16.8 mmol) of N-{5-(4-chlorophenyl)pent-1-en-4-yl}-3.5-dimethylbenzamide and 100 mg of benzyltributylammonium chloride in 15 ml of 50% strength aqueous sodium hydroxide solution and 15 ml of dichloromethane at 0°-5°. The organic phase is taken up in dichloromethane and water, the organic phase is separated off, dried over sodium sulfate and evaporated to dryness under reduced pressure. The oily residue is purified by chromatography on silica gel with ethyl acetate/hexane (1:4) as mobile phase; TLC (ethyl acetate/hexane; 1:3):Rf =0.50; 1H-NMR (300 MHz, CDCl3):mixture of rotamers, δ=7.31-7.18 (m, 4 H), 7.04-6.85 (m, 2.6 H), 6.42 (hr. s, 0.4 H), 5.92-5.60 (m, 1 H), 5.20-5.02 (m, 2 H), 4.54-4.24 (m, 2 H), 3.96-3.67 (m, 1 H), 3.25-2.40 (m, 6 H), 2.28 (s, ca 5 H), 2.24 (s, ca 1 H), 1.34-1.21(m, ca 0.5 H), 1.08 (t, J=7, ca 2.5 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646144
출처 데이터셋uspto-grants-1997_07
ORD IDord-fdce7d4e72c04bffb1204638a1122797
출처 메모uspto-grants-1997_07