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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54748생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/54748

반응식

참여 물질

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

반응 단계

15 ml of thionyl chloride was added to 0.44 g of 2-chlorophenylacetic acid. The mixture was stirred at room temperature for 2 hours. The reaction mixture was subjected to distillation to remove the remaining thionyl chloride and then to azeotropy with toluene twice to completely remove the thionyl chloride. The residue was dissolved in 10 ml of dichloromethane. 0.36 ml of triethylamine was added, with ice-cooling, to a dichloromethane solution containing 0.40 g of 5-dimethylamino-1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzoazepine. Thereto was dropwise added the above obtained 2-(2-chlorophenyl)acetyl chloride solution. The resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was water-washed twice, then dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (elutant: chloroform/methanol=200/1) and then recrystallized from methanol-diethyl ether to obtain 0.29 g of 5-dimethylamino-1-{4-[2-(2-chlorophenyl)acetylamino]benzoyl}-2,3,4,5-tetrahydro-1H-benzoazepine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622947
출처 데이터셋uspto-grants-1997_04
ORD IDord-d0c460ed1540444c85bf2a050d61eee3
출처 메모uspto-grants-1997_04