참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Bromide | HCID 6332 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 4-Hydroxy-4'-chlorobenzophenone | HCID 123504 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | HCID 178418443 | HCID 178418443 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcohol | HCID 14727318 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04508926 |
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| 출처 데이터셋 | uspto-grants-1985_04 |
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| ORD ID | ord-53d61037ce724e43bc1c56f669641de6 |
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| 출처 메모 | uspto-grants-1985_04 |
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