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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1850873생성일: 2026년 10월 25일

O-Methyltyramine → 1-(4-chlorophenyl)-N-[2-(4-methoxyphenyl)ethyl]cyclopropanecarboxamide

https://huagongshe.com/reaction/1850873

반응식

참여 물질

역할이름HCID투입량
반응물O-MethyltyramineHCID 4657—
반응물1-(p-Chlorophenyl)cyclopropanecarboxylic acidHCID 98606—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매WaterHCID 962—
생성물1-(4-chlorophenyl)-N-[2-(4-methoxyphenyl)ethyl]cyclopropanecarboxamideHCID 60409668—

반응 단계

A solution of 1-(4-chlorophenyl)cyclopropanecarboxylic acid (5.0 g, 25.3 mmol), 2-(4-methoxyphenyl)ethanamine (4.2 g, 28 mmol) and 4-N,N-Dimethylaminopyridin (3.3 g; 28 mmol) in methylenehloride (200 ml) was cooled to −10° C. N-ethyl-N′-(3-Dimethylaminopropyl)-carbodiimid hydrochloride (EDC, 5.3 g, 28 mmol) was added in several portions and the resulting mixture stirred overnight. The reaction mixture was poured into water and consecutively extracted with water, 2N NaOH and 1N HCl. Evaporation of the dried (NaSO4) extract yielded an oily residue that crystallized upon addition of n-heptan, which was used without further purification. Yield 7.0 g (21.2 mmol, 83%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08957089B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-bef0d4a902b649ad986996cdb96c4d6a
출처 메모uspto-grants-2015_02