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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704565생성일: 2026년 10월 24일

Hydrochloric Acid → 1-(o-Aminophenyl)-4-chloro-1-butanone hydrochloride

https://huagongshe.com/ko/reaction/704565

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl EtherHCID 3283—
반응물AnilineHCID 6115—
반응물4-ChlorobutyronitrileHCID 12336—
반응물Boron TrichlorideHCID 25135—
반응물Aluminum(III) ChlorideHCID 6451240—
용매1,2-DichloroethaneHCID 11—
생성물1-(o-Aminophenyl)-4-chloro-1-butanone hydrochlorideHCID 23293246—

반응 단계

To a solution of boron trichloride (55 g) in 1,2-dichloroethane (200 ml) at 0° was added dropwise a solution of aniline (39.1 g, 0.42 mol) in 1,2-dichlorolethane (50 ml) maintaining the temperature below 5°. On completion of the addition 4-chlorobutyronitrile (41.4 g, 0.42 mol) and aluminium chloride (53.34 g, 0.42 mol) were added successively and the reaction mixture allowed to warm up to room temperature then heated under reflux for 20 hours. After allowing to cool, 2N hydrochloric acid (100 ml) was added and the reaction mixture heated under reflux for 0.5 hour. The solid obtained was collected by filtration, taken up in water and extracted with chloroform (5×200 ml). The chloroform extracts were combined, washed with dilute base, then water, dried over magnesium sulphate, filtered and evaporated under reduced pressure to give an oil. The oil was dissolved in ether and ethanolic HCl was added, the resulting solid was collected by filtration and dried, 28.5 g. Recrystallization from ethanol/diethyl ether gave the product, m.p. 152-154°

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04988695
출처 데이터셋uspto-grants-1991_01
ORD IDord-1c5e3f2dfdf149f897471fb4864a7eb5
출처 메모uspto-grants-1991_01