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-Hydroxy-4'-chlorobenzophenone | HCID 123504 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | HCID 178418443 | HCID 178418443 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcohol | HCID 14727318 | — |
反応手順
To a solution of ethyl magnesium bromide prepared from 3.9 g. of magnesium turnings and 17.4 g. of ethyl bromide in 50 ml. of dry ether a solution of 9.3 g. of 4-chloro-4'-hydroxy-benzophenone in 40 ml. of dry ether is added dropwise, with stirring at -10° C., in nitrogen atmosphere. The reaction mixture is allowed to warm up to room temperature, stirred at this temperature for an additional half an hour, and is then poured onto a solution of ammonium chloride in ice water 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. After filtering the solvent is distilled off in vacuo, the residue is decolored with charcoal in methanol, the solution is filtered, and the solvent is evaporated under reduced pressure. The crude mixture is crystallized from a mixture of benzene and ethyl acetate to yield 5.5 g. of the named compound, melting at 148° to 149° 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-53d61037ce724e43bc1c56f669641de6 |
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| 出典メモ | uspto-grants-1985_04 |
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