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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 360030생성일: 2026년 10월 25일

Water → tert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoate

https://huagongshe.com/reaction/360030

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Diethyl EtherHCID 3283—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물Hexanoic acid, 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-oxo-, 1,1-dimethylethyl ester, (R)-(9CI)HCID 15045171—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoateHCID 9794547—

반응 조건

온도25 °C

반응 단계

A solution of crude (R)-1,1-dimethylethyl 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3oxohexanoate, 43 g (0.126 mol) in 350 mL of tetrahydrofuran is treated with 213 mL of tetrabutylammonium fluoride solution (1.0 M in hexane). The resulting mixture is stirred for five hours, at 25° C. The mixture is treated with 500 mL of water, 300 mL of diethyl ether is added, and the layers separated. The organic layer is dried (magnesium sulfate) and then filtered through a plug of silica gel with the aid of anhydrous diethyl ether. The solvent is removed under a vacuum to obtain 21 g of crude (R)-1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxohexanoate with acceptable NMR, MS and IR spectra.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05003080
출처 데이터셋uspto-grants-1991_03
ORD IDord-58f5e643b0c34929a98f180ed8cea65e
출처 메모uspto-grants-1991_03