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HRID 704565作成日:2026年10月26日

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

https://huagongshe.com/reaction/704565

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Diethyl EtherHCID 3283—
反応物AnilineHCID 6115—
反応物4-ChlorobutyronitrileHCID 12336—
反応物Boron TrichlorideHCID 25135—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒1,2-DichloroethaneHCID 11—
生成物1-(o-Aminophenyl)-4-chloro-1-butanone hydrochlorideHCID 23293246—

反応手順

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°

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04988695
出典データセットuspto-grants-1991_01
ORD IDord-1c5e3f2dfdf149f897471fb4864a7eb5
出典メモuspto-grants-1991_01