関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | 4-Methylbenzenethiol | HCID 7811 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | O-(p-toluenesulfonyl)-m-phenoxymandelonitrile | HCID 12945136 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | alpha-(p-Tolylthio)(m-phenoxyphenyl)-acetonitrile | HCID 12945139 | 100.7% |
反応手順
p-Toluenethiol (5.00 g) was dissolved in 6 ml of methanol, and 1.60 ml of a 2.5 M methanol solution of sodium methoxide was added to the solution at room temperature in a stream of argon. The mixture was stirred under ice cooling. Then, 1.516 g of O-(p-toluenesulfonyl)-m-phenoxymandelonitrile was added, and the mixture was stirred for 30 minutes under ice cooling and then for 10 minutes at room temperature. Water (20 ml) was added, and the mixture was extracted with 30 ml of methylene chloride three times. The extract was washed with 20 ml of water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel; benzene) to afford 1.334 g (yield 100%) of alpha-(p-tolylthio)(m-phenoxyphenyl)acetonitrile as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04340740 |
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| 出典データセット | uspto-grants-1982_07 |
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| ORD ID | ord-489135cf672b4e8e8213b4db717ccb32 |
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| 出典メモ | uspto-grants-1982_07 |
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