関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 3-(1-Piperidinylmethyl)phenoxy propanamine | HCID 21297576 | — |
| 触媒 | Mercuric Chloride | HCID 24085 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | [3-[3-(1-Piperidinylmethyl)phenoxy]propyl]isothiocyanate | HCID 13391620 | — |
反応手順
A solution of carbon disulphide (3.3 ml) in acetone (8 ml) was added dropwise to a solution of 3-[3-(1-piperidinylmethyl)phenoxy propanamine (12.4 g) in acetone (30 ml) over a 15 minute period, between -5° and -10° C. The solution was cooled to -14° C. and mercury (II) chloride (13.6 g) in acetone (30 ml) was added, during 45 minutes. Triethylamine (16 ml) was added at 0° C. during 15 minutes, and the mixture was heated at reflux for 45 minutes. The resulting suspension was purified by filtration and the filtrate evaporated in vacuo. The residue was purified by column chromatography using methanol as eluant to give the title compound (6 g) as an amber oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04764612 |
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| 出典データセット | uspto-grants-1988_08 |
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| ORD ID | ord-c5fa03e0c1ec46999ab8fa5c993f6693 |
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| 出典メモ | uspto-grants-1988_08 |
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