関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 3-(4-Phenylpiperazin-1-yl)propan-1-amine | HCID 261297 | — |
| 生成物 | methyl N-[3-(4-phenyl-1-piperazinyl)propyl]dithiocarbamate | HCID 12802957 | — |
反応手順
To a solution of potassium hydroxide (2.85 g) in methanol (25 ml) was added 3-(4-phenyl-1-piperazinyl)propylamine (11.1 g) and thereto was added carbon disulfide (3.85 g) under ice cooling over a period of 10 minutes. The resulting mixture was stirred for 3 hours under ice cooling. The reaction mixture was evaporated under reduced pressure. The residual oil was dissolved in water (40 ml) and washed with diethyl ether. The washed aqueous layer was ice-cooled and thereto was added methyl iodide (7.2 g) with stirring. The resulting mixture was stirred for 2 hours under ice-cooling and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and then evaporated to give methyl N-[3-(4-phenyl-1-piperazinyl)propyl]dithiocarbamate (12.9 g), mp 75° to 79° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04443443 |
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| 出典データセット | uspto-grants-1984_04 |
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| ORD ID | ord-47a37082f86147eb8754f6b794732fcd |
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| 出典メモ | uspto-grants-1984_04 |
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