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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1022464생성일: 2026년 10월 27일

Triethylsilane → 6-(2-Bromo-5-iodobenzyl)-2,3-dihydrobenzo[b][1,4]dioxine

https://huagongshe.com/reaction/1022464

반응식

참여 물질

역할이름HCID투입량
반응물TriethylsilaneHCID 12052—
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물Methanone, (2-bromo-5-iodophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)-HCID 58340798—
촉매Trifluoromethanesulfonic acidHCID 62406—
용매Trifluoroacetic acidHCID 6422—
생성물6-(2-Bromo-5-iodobenzyl)-2,3-dihydrobenzo[b][1,4]dioxineHCID 5834083084.3%

반응 단계

(Note: This reaction was done in 5 lit. R. B. flask). To a stirred solution of (2-bromo-5-iodo-phenyl)-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-methanone (180 g, 404.49 mmol) in trifluoroacetic acid (600 ml) was added triethylsilane (386.5 ml, 2426.9 mmol) followed by triflic acid (2.3 ml) at room temperature (note: after addition of 1 drop of triflic acid exotherm was observed so addition was done very slowly in such a way that reaction mixture refluxed gently). After stirring for 25 min at room temperature, volatiles were evaporated under reduced pressure. The resulting residue was taken in ethyl acetate (1500 ml) and washed with saturated aqueous sodium bicarbonate solution (1000 ml×2), water (1000 ml), brine (1000 ml), dried over sodium sulfate, and concentrated. The resulting residue was triturated with hexane. The residue was recrystallized from ethanol to give 147 g of 6-(2-bromo-5-iodo-benzyl)-2,3-dihydro-benzo[1,4]dioxine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722633B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-88c1275bcfb444548127d9b446d8a601
출처 메모uspto-grants-2014_05