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4,4'-Dichlorobutyrophenone → 1-(4-Chlorophenyl)-4-[4-[3-chloro-4-(hydroxymethyl)phenyl]-1-piperazinyl]-1-butanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4,4'-Dichlorobutyrophenone | HCID 2723781 | — |
| 反応物 | 2-Chloro-4-(1-piperazinyl)benzenemethanol | HCID 13457101 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 1-(4-Chlorophenyl)-4-[4-[3-chloro-4-(hydroxymethyl)phenyl]-1-piperazinyl]-1-butanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04515793 |
| 出典データセット | uspto-grants-1985_05 |
| ORD ID | ord-cc769d2e0e8d40df8c844ef0c645c1d1 |
| 出典メモ | uspto-grants-1985_05 |