関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl Bromide | HCID 6332 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 4-Fluoro-4'-hydroxybenzophenone | HCID 117666 | — |
| 反応物 | Lithium | HCID 3028194 | — |
| 反応物 | HCID 178506846 | HCID 178506846 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrol | HCID 14727320 | — |
反応手順
To a solution of ethyl lithium prepared from 2.8 g. of lithium metal and 21.8 g. of ethyl bromide in 265 ml. of dry ether a solution of 10.8 g. of 4-fluoro-4'-hydroxy-benzophenone in 50 ml. of dry tetrahydrofurane is added dropwise, with stirring in argon atmosphere, at a temperature between -40° C. and -30° C. When the addition is complete, the mixture is allowed to warm up to 0° C., and is then stirred at this temperature for further 30 minutes. The mixture is decomposed with a 20% aqueous ammonium chloride solution under cooling. The aqueous phase is extracted with ether, the ethereal phases are combined, washed to neutral with water, and dried over anhydrous magnesium sulfate. The solution is evaporated under reduced pressure, and the solid residue is crystallized from a mixture of n-hexane and ethyl acetate to yield 8.2 g. of the named product, melting at 125° to 126° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04508926 |
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| 出典データセット | uspto-grants-1985_04 |
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| ORD ID | ord-917d616c80ac4359ad0270951878f8b6 |
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| 出典メモ | uspto-grants-1985_04 |
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