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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222464생성일: 2026년 10월 25일

Imidazole → 6-(Tert-butyl-diphenyl-silanyloxy)-benzofuran-3-one

https://huagongshe.com/reaction/222464

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
반응물6-Hydroxy-3-coumaranoneHCID 235717—
용매DichloromethaneHCID 6344—
용매Sodium chloride; waterHCID 57417360—
생성물6-(Tert-butyl-diphenyl-silanyloxy)-benzofuran-3-oneHCID 68526161—

반응 단계

To a solution of 6-hydroxy-benzofuran-3-one (1.01 g, 6.73 mmol) in dry dichloromethane (18 mL) was added imidazole (0.458 g, 6.727 mmol) followed by tert-butyldiphenylchlorosilane (1.72 mL, 6.73 mmol) at room temperature. The mixture was stirred overnight and poured into brine. The aqueous phase was extracted with dichloromethane. The combined organic layers were dried over Na2SO4, evaporated in vacuo and the residue was purified by column chromatography (ethylacetate:hexane; 1:9) to give the 6-(tert-butyl-diphenyl-silanyloxy)-benzofuran-3-one as slightly yellow oil (1.34 g, 52%). 1H NMR (CDCl3, 400 MHz) 1.21 (s, 9H), 4.54 (s, 2H), 6.40 (s, 1H), 6.55 (dd, J=1.6, 8.0 Hz, 1H), 7.38-7.50 (m, 7H), 7.67 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207216B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-6079800153794aac983a1ae9d9c44a76
출처 메모uspto-grants-2012_06