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Hydrochloric Acid → 1-(o-Chlorophenoxy)-4-(4-phenyl-1-piperazinyl)-2-butanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 1-Phenylpiperazine | HCID 7096 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 1-(o-Chlorophenoxy)-2-hydroxybutyl chloride | HCID 19840239 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 1-(o-Chlorophenoxy)-4-(4-phenyl-1-piperazinyl)-2-butanol | HCID 13120451 | — |
反応手順
A mixture of 35.1 g. (0.15 mole) of 1-(o-chlorophenoxy)-2-hydroxybutyl chloride, 32.6 g. (0.2 mole) of N-phenylpiperazine and 400 ml. of isopropanol was refluxed for 48 hr. The reaction mixture was allowed to stand in a refrigerator overnight and filtered. The filtrate was treated with ethereal hydrogen chloride and the salt precipitated by the addition of ether. The white crystalline solid which formed was dissolved in 0.1 mole of hydrochloric acid and then neutralized with sodium hydroxide producing a crystalline precipitate. This was recrystallized with isopropanol yielding 36 g. of the free base of the product which melted at 100°-101.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04609735 |
| 出典データセット | uspto-grants-1986_09 |
| ORD ID | ord-a63c9a72ac364cb3ad8467f039c0d8f8 |
| 出典メモ | uspto-grants-1986_09 |