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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

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 2-methyl-4,4,4-trifluoroacetoacetateHCID 2737204—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
생성물Ethyl 3-hydroxy-2-methyl-4,4,4-trifluorobutyrateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06130315
출처 데이터셋uspto-grants-2000_10
ORD IDord-17d7ea44ea634f2fbf32a772f4911a8c
출처 메모uspto-grants-2000_10