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Pyridine → 6-(1-Bromoethyl)-4,4-dimethylchroman
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Phosphorus tribromide | HCID 24614 | — |
| 反応物 | 4,4-Dimethyl-6-(1-hydroxyethyl)chroman | HCID 14010248 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 6-(1-Bromoethyl)-4,4-dimethylchroman | HCID 14010250 | 153.7% |
反応手順
To a stirred solution of 6.0 g (29.1 mmol) of 4,4-dimethyl-6-(1-hydroxyethyl)chroman and 1.15 g (14.5 mmol) of pyridine in 25 ml of hexane, was added 3.92 g (14.5 mmol) of phosphorus tribromide, at ca. 0° C. Stirring was continued at ca. 0° C. for 1 hour, and then the reaction mixture was poured into 500 ml of diethyl ether. The ether was washed with water, dried (MgSO4) and evaporated in vacuo to give 6.0 g (78% yield) of the title compound as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04808597 |
| 出典データセット | uspto-grants-1989_02 |
| ORD ID | ord-2a1342534fe24399a8def04da785ad83 |
| 出典メモ | uspto-grants-1989_02 |