Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 366928생성일: 2026년 10월 25일
Ethyl 2-methyl-4,4,4-trifluoroacetoacetate → Ethyl 3-hydroxy-2-methyl-4,4,4-trifluorobutyrate
https://huagongshe.com/reaction/366928
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 2-methyl-4,4,4-trifluoroacetoacetate | HCID 2737204 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Ethyl 3-hydroxy-2-methyl-4,4,4-trifluorobutyrate | HCID 533787 | — |
반응 단계
To a solution of ethyl 3-keto-2-methyl-4,4,4-trifluorobutanoate (20.1 g, 0.10 moles) in 250 ml of absolute ethanol, cooled in an ice bath, was added sodium borohydride (1.0 g, 0.25 moles) in portions with stirring. The cooling bath was removed and the reaction stirred at room temperature for 30 minutes. Acetone (5 ml) was added to quench any remaining sodium borohydride and the solvents removed by distillation at atmospheric pressure using a Vigreaux column. The residue was diluted with 200 ml of methylene chloride and poured into a separatory funnel containing 75 ml of a 1:1:1 mixture of saturated ammonium chloride:brine:water. The layers were separated and the aqueous phase extracted with methylene chloride (3×25 ml). The combined organic phase and methylene chloride extracts were dried over magnesium sulfate, filtered and distilled at atmospheric pressure to remove the solvents. The residue was then distilled at reduced pressure (20 mmHg) using a Vigreaux column to give ethyl 3-hydroxy-2-methyl-4,4,4-trifluorobutanoate, bp 78-84° C., 20 mmHg.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06130315 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-17d7ea44ea634f2fbf32a772f4911a8c |
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| 출처 메모 | uspto-grants-2000_10 |
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