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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380052생성일: 2026년 10월 25일

Imidazole → (3R,4S)-3-[4-(4-Bromophenoxy)-3-(t-butyldimethylsilanyloxy)hexyl]pyridine

https://huagongshe.com/reaction/380052

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물(3r,4s)-4-(4-Bromophenoxy)-1-pyridin-3-yl-hexan-3-olHCID 57271083—
용매DimethylformamideHCID 6228—
생성물(3R,4S)-3-[4-(4-Bromophenoxy)-3-(t-butyldimethylsilanyloxy)hexyl]pyridineHCID 5709086540%

반응 조건

온도50 °C

반응 단계

To a solution of (3R,4S)-4-(4-bromophenoxy)-1-pyridin-3-yl-hexan-3-ol (1.34 g, Example 87d)) in dry N,N-dimethylformamide (30 ml) was added tertbutyldimethylsilyl chloride (0.80 g) and imidazole (0.77 g) and the resulting solution heated at 50° C. for 20 hours. The solution was concentrated in vacuo. The residue was made basic by addition of saturated sodium hydrogen carbonate solution and extracted with ethyl acetate. The combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography over silica eluting with ethyl acetate:isohexane (1:1) to give the sub-title compound as an oil (0.71 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300352B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-8f101bee1e1445f181fbec58fa541093
출처 메모uspto-grants-2001_10