참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 1-(3,4-Dichlorophenyl)-1-cyclobutane-carbonitrile | HCID 10857134 | — |
| 반응물 | HCID 178418373 | HCID 178418373 | — |
| 생성물 | 1-Acetyl-1-(3,4-dichlorophenyl)cyclobutane | HCID 13083139 | — |
반응 단계
A solution of 1-(3,4-dichlorophenyl)cyclobutanecarbonitrile (163.6 g) in ether (130 ml) was added dropwise over 0.5 hours at ambient temperature under nitrogen to stirred methylmagnesium iodide (3M solution in ether; 300 ml), then the mixture was heated under reflux for 1 hour, diluted with ether (100 ml), heated under reflux for a further 2.5 hours, then stirred at ambient temperature for 18 hours. The resulting solid was collected by filtration, washed well with ether, and added in portions at <20° C. to a stirred mixture of concentrated hydrochloric acid (410 ml) and water (650 ml). The mixture was heated at 95° C. for 0.5 hours with occasional stirring then cooled to ambient temperature. The product was extracted into dichloromethane (3×200 ml), the combined extracts were dried over magnesium sulphate, and the solvent removed in vacuo to leave 1-[1-(3,4-dichlorophenyl)-cyclobutyl]ethanone as a dark red oil (172.7 g) which was used without purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05652271 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-38cae80a86894793a74ce171ca39aa60 |
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| 출처 메모 | uspto-grants-1997_07 |
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