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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 | 4-Bromobutanol | HCID 118388 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 2-(4-Bromobutoxy)tetrahydro-2H-pyran | HCID 559019 | 96% |
反応手順
16.0 g (105.0 mmols) of 4-bromobutanol was dissolved in 140 ml of chloroform, and a solution prepared by dissolving 13.9 ml (1.5-fold equivalent weight) of 3,4-dihydro-2H-pyran in 40 ml of chloroform was dropwise added thereto at 0° C. in an atmosphere of argon. The solution obtained was stirred for 4 hours while keeping it at 0° C., followed by addition of an aqueous sodium hydrogencarbonate, and the resulting solution was extracted with chloroform (100 ml×2). The organic layer obtained was dried with anhydrous sodium sulfate, and thereafter concentrated under reduced pressure to obtain 24.0 g of 4-(tetrahydropyran-2-yl)oxybutyl bromide (yield: 96%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05834575 |
| 出典データセット | uspto-grants-1998_11 |
| ORD ID | ord-b64c65c0f2384dae8d897b7ee6eef632 |
| 出典メモ | uspto-grants-1998_11 |