참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzyl 2,2,2-trichloroacetimidate | HCID 144968 | — |
| 반응물 | Butanoic acid, 3-hydroxy-, ethyl ester, (3S)- | HCID 6950306 | — |
| 촉매 | Trifluoromethanesulfonic acid | HCID 62406 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (3S)-3-(benzyloxy)butanoic acid ethyl ester | HCID 14201835 | 200.7% |
반응 단계
Under a nitrogen atmosphere, to a solution of (S)-(+)-3-hydroxybutyric acid ethyl ester (100 g, 0.76 mol) in methylene chloride (1.0 L), benzyl 2,2,2-trichloroacetoimidate (381 g, 1.5 mol) and trifluoromethanesulfonic acid (6.7 mL, 76 mmol) were gradually added, and the mixture was stirred at room temperature overnight. The precipitated solid was filtered, and after the mother liquid was successively washed with a saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, it was dried with sodium sulfate and the solvent was distilled off under reduced pressure. Hexane was added to the residue, and after the solid was filtered again, the solvent of the mother liquid was distilled off under reduced pressure to give (3S)-3-(benzyloxy)butanoic acid ethyl ester (339 g) as a mixture. The present compound was used for the subsequent reaction without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642640B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-8f6474ba20e846e49214da9fa1a069b8 |
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| 출처 메모 | uspto-grants-2014_02 |
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