関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | 2-tert-Butyl-6-methylphenol | HCID 16678 | — |
| 反応物 | Tin tetrachloride | HCID 24287 | — |
| 反応物 | Hex-5-ynoyl chloride | HCID 2759284 | — |
| 生成物 | 2-t-Butyl-4-(5-hexynoyl)-6-methylphenol | HCID 14672032 | 51.4% |
反応手順
To a solution of 2-tert-butyl-6-methylphenol (1.2 g, 7.3 mmol) in methylene chloride (28 ml, 1.1 equiv.), stirred under argon at -78° C., is added 5-hexynoyl chloride (1.0 g) followed by tin tetrachloride (0.93 mL, 1.1 equiv.). After stirring 30 minutes at -78° C., the reaction is warmed to -50° C. and stirred 5 minutes more. The mixture is then quenched with 1N HCl/ether. The product is extracted from 1N HCl with 3 portions of ether, and the ether layers are combined and washed with water. The resulting ether layer is dried (MgSO4), filtered, and concentrated in vacuo to give 2.14 g crude product. The product is flash chromatographed on silica gel using 10% EtOAc in hexane to give 0.97 g 2-t-butyl-4-(5-hexynoyl)-6-methylphenol. Crystallization from hexane gives crystals, mp 63°-64° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04847303 |
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| 出典データセット | uspto-grants-1989_07 |
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| ORD ID | ord-97253f98aac7407fa153e1b9d13dad5b |
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| 出典メモ | uspto-grants-1989_07 |
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