참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Hydrogen Bromide | HCID 260 | — |
| 반응물 | 3-Hydroxybutyrolactone, (3S)- | HCID 7269389 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (3S)-3-acetyloxy-4-bromobutanoic acid | HCID 2733880 | 95% |
반응 단계
To a 2 l of three-necked flask equipped with reflux condenser, thermometer and mechanical stirrer were charged (S)-3-hydroxy-γ-butyrolactone (102 g) and 30% of hydrobromic acid in acetic acid (675 g, 2.5 eq.). The mixture was stirred at 40° C. for 3 hours. After cooling the reaction mixture, methylene chloride (1000 ml) was added to it. The reaction mixture was washed with aqueous solution of sodium acetate. The organic layer was separated, dried over magnesium sulfate, and concentrated to afford (S)-3-acetoxy-4-bromobutyric acid (213 g, 95%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06586616B1 |
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| 출처 데이터셋 | uspto-grants-2003_07 |
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| ORD ID | ord-811ace35f479451696a4894ed030bdba |
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| 출처 메모 | uspto-grants-2003_07 |
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