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p-Toluenesulfonic acid → 4-(2,3-Difluorophenoxy)-butan-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 2-[4-(2,3-Difluorophenoxy)butoxy]-tetrahydropyran | HCID 22016256 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | MeOH tetrahydrofuran | HCID 21899815 | — |
| 生成物 | 4-(2,3-Difluorophenoxy)-butan-1-ol | HCID 22016257 | — |
反応手順
To a solution of 2-[4-(2,3-difluorophenoxy)-butoxy]-tetrahydropyran (20) (1 equi.) and commercially available para-toluenesulfonic acid (21) (0.1 equi.) in methanol:THF (1:1) (3 mL/mmole), water (0.005 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h, quenched with water, extracted with ethyl acetate:hexane (1:1), washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (10% EtOAc/hexanes) gave 4-(2,3-difluorophenoxy)-butan 1-ol (22), as a white solid (84%)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07083832B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-1f6cb91870914577b79f39714d7ce277 |
| 出典メモ | uspto-grants-2006_08 |