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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5582생성일: 2026년 10월 23일

o-Chlorophenylacetic acid → Acetyl chloride, 2-(2-chlorophenyl)-

https://huagongshe.com/ko/reaction/5582

반응식

참여 물질

역할이름HCID투입량
반응물o-Chlorophenylacetic acidHCID 17124—
반응물Thionyl ChlorideHCID 24386—
생성물Acetyl chloride, 2-(2-chlorophenyl)-HCID 182669—

반응 단계

To 2-chlorophenylacetic acid (0.44 g) is added thionyl chloride (15 ml), and the mixture is stirred at room temperature for 2 hours. Thionyl chloride is distilled off, and the resultant is further distilled off by subjecting twice to azeotrophy with toluene. The resulting residue is dissolved in dichloromethane (10 ml). Separately, to a solution of 5-dimethylamino-1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (0.40 g) in dichloromethane is added triethylamine (0.36 ml) under ice-cooling, and thereto is added dropwise the above obtained 2-(2-chlorophenyl)acetyl chloride solution. After addition, the mixture is stirred at room temperature for one hour, washed twice with water, dried over magnesium sulfate, and concentrated. The resulting residue is purified by silica gel column chromatography (eluent; chloroform:methanol=200:1), and recrystallized from methanol/diethyl ether to give 5-dimethylamino-1-{4-[2-(2-chlorophenyl)acetylamino]benzoyl}-2,3,4,5-tetrahydro-1H-benzazepine (0.29 g) as white powder, mp. 187°-189° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244898
출처 데이터셋uspto-grants-1993_09
ORD IDord-3db121cfac504d159b1b06562cabf306
출처 메모uspto-grants-1993_09