참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Ethyl Acetoacetate | HCID 8868 | — |
| 반응물 | Magnesium Chloride | HCID 5360315 | — |
| 반응물 | 2,2-Dimethyl-3-phenylpropanoyl chloride | HCID 13307229 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Ethyl 4,4-dimethyl-3-oxo-5-phenylpentanoate | HCID 86697460 | 18% |
반응 단계
Ethyl 3-oxobutanoate (1.09 g, 8.3 mmol) in methylene chloride (16 mL) was mixed with anhydrous magnesium chloride (158 mg, 1.66 mmol), and the reaction solution was cooled to 0° C., mixed with pyridine (1.34 mL, 16.6 mmol), stirred for 30 minutes, then mixed with 2,2-dimethyl-3-phenylpropanoyl chloride (1.64 g, 8.3 mmol) and stirred for another 30 minutes at the same temperature. The reaction solution was warmed to room temperature and stirred for 20 hours. The methylene chloride was distilled off under reduced pressure, and the residue was with ethanol (2 mL) and at room temperature for 2 days and with toluene (2 mL) at 60° C. for 5 hours. After completion of the reaction, the reaction solution was washed with saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate (50 mL×2). The solvent was removed from the resulting organic layer under reduced pressure, and the resulting brown oil was purified by intermediate pressure silica gel column chromatography (silica gel12 g, ethyl acetate:hexane=1:19 to 1:9) to give 370 mg of the desired product as a light brown oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08658686B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-f310f4dcb6274a00b1d15af426616c40 |
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| 출처 메모 | uspto-grants-2014_02 |
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