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HRID 1022464作成日:2026年10月27日

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

https://huagongshe.com/reaction/1022464

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylsilaneHCID 12052—
反応物Trifluoromethanesulfonic acidHCID 62406—
反応物Methanone, (2-bromo-5-iodophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)-HCID 58340798—
触媒Trifluoromethanesulfonic acidHCID 62406—
溶媒Trifluoroacetic acidHCID 6422—
生成物6-(2-Bromo-5-iodobenzyl)-2,3-dihydrobenzo[b][1,4]dioxineHCID 5834083084.3%

反応手順

(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722633B2
出典データセットuspto-grants-2014_05
ORD IDord-88c1275bcfb444548127d9b446d8a601
出典メモuspto-grants-2014_05