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p-Toluenesulfonic acid → (RS)-2-(2-buten-1-yl)-6-chloro-1-indanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 3-Buten-2-ol | HCID 11716 | — |
| 反応物 | 6-Chloro-1-indanone | HCID 5100705 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | 2,2-Dimethoxypropane | HCID 6495 | — |
| 生成物 | (RS)-2-(2-buten-1-yl)-6-chloro-1-indanone | HCID 54260426 | 39% |
反応手順
A solution of 20.2 g of 6-chloro-1-indanone, 25 ml of 3-buten-2-ol and 200 mg of p-toluenesulfonic acid in 25 ml of 2,2-dimethoxypropane and 200 ml of anhydrous toluene was boiled under reflux for 16 hours. The reaction mixture was subsequently concentrated in a vacuum and purified by column chromatography on silica gel (hexane/diethyl ether 5:1). 10.3 g (39%) of (RS)-2-(2-buten-1-yl)-6-chloro-1-indanone were obtained as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05646173 |
| 出典データセット | uspto-grants-1997_07 |
| ORD ID | ord-5f8c9b4d66fb4219af2fa3d5e6bc72aa |
| 出典メモ | uspto-grants-1997_07 |