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3,4-dihydro-2H-pyran → 2-(4-Bromobutoxy)tetrahydro-2H-pyran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-Bromobutanol | HCID 118388 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Phosphorus oxychloride | HCID 24813 | — |
| 生成物 | 2-(4-Bromobutoxy)tetrahydro-2H-pyran | HCID 559019 | — |
反応手順
To a solution of commercially available 4-bromobutan-1-ol (16) (1 equi.) and 3,4-dihydropyran (17) (1.5 equi.) in dichloromethane (3 mL/mmole), phosphorus oxychloride (0.01 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h. Then potassium carbonate (1 equi.) was added to the reaction mixture and the reaction mixture was stirred at room temperature for 1 h, quenched with water, extracted with dichloromethane, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (5% EtOAc/hexanes) afforded 2-(4-bromobutoxy)-tetrahydropyran (18), as a colorless oil (88%).
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-897b02d40a5c415e94fa7c6fe1ac97fb |
| 出典メモ | uspto-grants-2006_08 |