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HRID 965338생성일: 2026년 10월 26일

Imidazole → 3-(Tert-butyldimethylsilyl)oxy-1-cyclohexanol

https://huagongshe.com/reaction/965338

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물1,3-CyclohexanediolHCID 10433—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물3-(Tert-butyldimethylsilyl)oxy-1-cyclohexanolHCID 55707750.6%

반응 단계

To a solution of 1,3-cyclohexanediol (cis and trans mixture, 25 g) and imidazole (8.8 g) in a mixture of dichloromethane (150 ml) and tetrahydrofuran (150 ml) was added dropwise a solution of tert-butyldimethylsilyl chloride (16.2 g) in a mixture of dichloromethane (40 ml) and tetrahydrofuran (40 ml) at 0° C. A reaction mixture was allowed to warm to ambient temperature and stirred overnight. Insoluble material was removed by filtration and mother liquor was concentrated under reduced pressure to give residue, which was dissolved in ethyl acetate (300 ml) and washed in turn with 1N-aqueous hydrochloric acid (100 ml), brine (100 ml), saturated sodium hydrogen carbonate in water (100 ml), and saturated sodium chloride in water, and dried over magnesium sulfate. Evaporation of the solvent gave a residue, which was chromatographed on silica gel (500 ml) eluting in turn with 10% and 20% ethyl acetate in n-hexane to give 3-(tert-butyldimethylsilyl)oxy-1-cyclohexanol (cis and trans mixture) (12.52 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05773530
출처 데이터셋uspto-grants-1998_06
ORD IDord-51c8a8f9bafa4f99882a38338689fb8a
출처 메모uspto-grants-1998_06