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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 500346생성일: 2026년 10월 25일

Imidazole → (R)-5-[(tert-Butyldiphenylsilyl)hydroxymethyl]-dihydro-2(3H)-furanone

https://huagongshe.com/reaction/500346

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
반응물(5R)-Dihydro-5-(hydroxymethyl)-2(3H)-furanoneHCID 6950353—
용매DimethylformamideHCID 6228—
생성물(R)-5-[(tert-Butyldiphenylsilyl)hydroxymethyl]-dihydro-2(3H)-furanoneHCID 6845909598%

반응 단계

To a solution of 3 (7.0 g, 60 mmol) and imidazole (9.19 g, 135 mmol) in anhydrous DMF (70 mL) was added tert-butyldiphenylsilyl chloride (18.14 g, 66 mmol, 17.2 mL), and the solution was stirred at room temperature under nitrogen atmosphere for 1 h. After removal of the solvent by evaporation, the residue was dissolved in CHCl3, washed with water and brine, dried (Na2SO4), filtered, and concentrated. After crystallization from hexane, the oily residue gave the title compound 4 as a white crystalline solid (20.8 g, 98%). M.P. 76° C.; 1H NMR (CDCl3) δ 7.68-7.65 (m, 4H, arom.), 7.47-7.39 (m, 6H, arom.), 4.63-4.61 (m, 1H, H-5), 3.90-3.87 (dd, J=3 & 11 Hz, 1H, CH2OH), 3.70-3.67 (dd, J=3 & 11 Hz, 1H, CH2OH), 2.69-2.65 (m, 1H, H-3), 2.56-2.52 (m, 1H, H-3), 2.32-2.23 (m, 2H, H-4), 1.06 (s, 9H, t-Bu).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772208B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-8b0c2c38c9fb4f71ab0c586d18fd323e
출처 메모uspto-grants-2010_08