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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1859002생성일: 2026년 10월 26일

Imidazole → (4aR,5S,8aS)-5-(tert-Butyl-dimethyl-silanyloxy)-8a-methyl-octahydro-naphtalen-1-one

https://huagongshe.com/reaction/1859002

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물N-ButylchlorodimethylsilaneHCID 66079—
반응물HCID 21309363HCID 21309363—
용매DimethylformamideHCID 6228—
생성물(4aR,5S,8aS)-5-(tert-Butyl-dimethyl-silanyloxy)-8a-methyl-octahydro-naphtalen-1-oneHCID 21309364—

반응 조건

온도100 °C

반응 단계

To a solution of 2.3 g (12.6 mMol) of (4aR,5S,8aS)-5-hydroxy-8a-methyl-octahydro-naphtalen-1-one in 63 ml of dimethylformamide are added under stirring and argon atmosphere 3.74 g (24.8 mMol) of tertio-butyl-dimethyl-silylchloride and 1.94 g (28.5 mMol) of imidazole. The reaction mixture is heated to 100° C. for 4 hours, then additional 3.74 g of tert-butyl-dimethylsilylchloride and 1.94 g of imidazole are added and the reaction mixture is kept overnight at 100° C. The reaction mixture is poured onto ice-water and extracted three times with diethylether. The combined organic extract is washed once with water and brine, dried over sodium sulfate and evaporated in vacuo. The residue is chromatographed over 250 g of silicagel with hexane/ethylacetate 9/1 to yield 3.17 g (85%) of low melting cristalline (4aR,5S,8aS)-5-(tert-butyl-dimethyl-silanyloxy)-8a-methyl-octahydro-naphtalen-1-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06153605
출처 데이터셋uspto-grants-2000_11
ORD IDord-b4d0def3c575404bab48d32938b0fa1c
출처 메모uspto-grants-2000_11