참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 2-(4'-Bromobiphenyl-4-yl)-N-methoxy-N-methylacetamide | HCID 86670083 | — |
| 반응물 | HCID 178418348 | HCID 178418348 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (4'-Bromobiphenyl-4-yl)acetone | HCID 68193283 | 71% |
반응 단계
A solution of methyllithium in diethyl ether (40 mL, 44 mmol) was diluted with tetrahydrofuran (120 mL), and a solution of 2-(4′-bromobiphenyl-4-yl)-N-methoxy-N-methylacetamide (12 g, 37 mmol) in tetrahydrofuran (50 mL) was added at −78° C., followed by stirring at the same temperature for 30 minutes. Water was added to the reaction solution, followed by extraction with ethyl acetate, and subsequently the solvent was distilled off under reduced pressure. The resulting residue was purified by chromatography on a silica gel column (Moritex Corporation, elution solvent: hexane/ethyl acetate), and a fraction corresponding to the Rf value=0.50 (hexane/ethyl acetate=4/1) by thin layer chromatography was concentrated under reduced pressure to afford the title compound (7.6 g, 26 mmol) as a white solid (yield 71%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08785462B2 |
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| 출처 데이터셋 | uspto-grants-2014_07 |
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| ORD ID | ord-8ff3149660df468d9359fbab80b4db33 |
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| 출처 메모 | uspto-grants-2014_07 |
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