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HRID 15347생성일: 2026년 10월 26일

Imidazole → 4-(((tert-Butyldimethylsilyl)oxy)methyl)-2-chloro-6-methoxypyridine

https://huagongshe.com/reaction/15347

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물WaterHCID 962—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물(2-Chloro-6-methoxypyridin-4-yl)methanolHCID 11457961—
용매DimethylformamideHCID 6228—
생성물4-(((tert-Butyldimethylsilyl)oxy)methyl)-2-chloro-6-methoxypyridineHCID 5748688893%

반응 단계

A solution of [2-chloro-6-(methyloxy)-4-pyridinyl]methanol (for a synthesis see Adamczyk, M.; Akireddy, S. R.; Reddy, Rajarathnam E. Tetrahedron 2002, 58(34), 6951)(8.02 g, 46.22 mmol) in dry DMF (100 ml) was treated with tert-butyldimethylsilyl chloride (8.36 g, 55.46 mmol) and imidazole (3.77 g, 55.46 mmol) and stirred at rt for 2 h. The reaction mixture was treated with water extracted three times with dichloromethane, dried (magnesium sulphate), evaporated and chromatographed on silica gel (100 g), eluting with 1:4 ethyl acetate-hexane to give the desired product (12.38 g, 93%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732461B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-882eac7cbb6649c0b1d8d9439948d79d
출처 메모uspto-grants-2010_06