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4-Toluenesulfonyl chloride → (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | (2S)-(4E)-5-(3-Pyridyl)-4-penten-2-ol | HCID 20655737 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonate | HCID 87465994 | 68.6% |
反応手順
Under a nitrogen atmosphere, p-toluenesulfonyl chloride (7.01 g, 36.77 mmol) was added to a stirring solution of (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol (3.00 g, 18.38 mmol) in dry triethylamine (20 mL) at 0° C. After stirring and warming to ambient temperature over 18 h, the mixture was stirred with cold, saturated NaHCO3 solution (50 mL) for 1 hour and extracted with chloroform (3×50 mL). The combined chloroform extracts were dried (K2CO3), filtered, and concentrated by rotary evaporation to afford a thick, dark-brown mass (˜7 g). The crude product was purified by column chromatography on silica gel, eluting with chloroform-acetone (98:2, v/v) to afford 4.00 g (68.6%) of a light-brown syrup.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06979695B2 |
| 出典データセット | uspto-grants-2005_12 |
| ORD ID | ord-078c4ce6f95e4e448f83fe237a725ad8 |
| 出典メモ | uspto-grants-2005_12 |