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HRID 462426作成日:2026年10月26日

4,4'-Dichlorobutyrophenone → 1-(4-Chlorophenyl)-4-[4-[3-chloro-4-(hydroxymethyl)phenyl]-1-piperazinyl]-1-butanone

https://huagongshe.com/reaction/462426

反応式

関与物質

役割名称HCID仕込み量
反応物4,4'-DichlorobutyrophenoneHCID 2723781—
反応物2-Chloro-4-(1-piperazinyl)benzenemethanolHCID 13457101—
溶媒AcetoneHCID 180—
溶媒TriethylamineHCID 8471—
生成物1-(4-Chlorophenyl)-4-[4-[3-chloro-4-(hydroxymethyl)phenyl]-1-piperazinyl]-1-butanoneHCID 13457142—

反応手順

A solution of 4,4'-dichlorobutyrophenone (4.5 g, 20.7 mmole) in 25 ml of acetone was added to a warm suspension of 2-chloro-4-(1-piperazinyl)benzenemethanol (4.7 g, 20.7 mole) in 50 ml acetone and 2.5 ml of triethylamine. The reaction mixture was refluxed for four days, cooled at -10° for three hours, and then filtered. The product was washed with a little acetone, triturated on the filter with water (four times, 50 ml), and air dried. Recrystallization from acetonitrile (65 ml) gave 3.0 g (35%), mp 137°-139°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04515793
出典データセットuspto-grants-1985_05
ORD IDord-cc769d2e0e8d40df8c844ef0c645c1d1
出典メモuspto-grants-1985_05