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HRID 221150作成日:2026年10月25日

Water → (5-Bromo-2-chlorobenzyloxy)(tert-butyl)diphenylsilane

https://huagongshe.com/reaction/221150

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物DiisopropylethylamineHCID 81531—
反応物tert-ButyldiphenylchlorosilaneHCID 94078—
反応物(5-Bromo-2-chlorophenyl)methanolHCID 5074766—
溶媒DimethylformamideHCID 6228—
生成物(5-Bromo-2-chlorobenzyloxy)(tert-butyl)diphenylsilaneHCID 57516661—

反応手順

To a solution of 5-Bromo-2-chlorobenzylalcohol (5.15 g) in N,N-dimethylformamide (50 ml) was added diisopropylethylamine (19.8 ml) and tert-butyldiphenylchlorosilane (11.9 ml), and the mixture was stirred at room temperature for 2 days. Under ice-cooling, to the mixture was added water, and the mixture was extracted with ethyl acetate. The extract was washed with successively with 0.4 M aqueous hydrochloric acid solution (twice), water, a saturated aqueous sodium hydrogen carbonate solution and brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by an aminosilane-treated silica gel column chromatography (hexane) to give 5-bromo-2-chloro-1-(tert-butyldiphenylsiloxymethyl)benzene 77 (10.79 g) as colorless oil. APCI-Mass m/Z 476/478 (M+NH4).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202984B2
出典データセットuspto-grants-2012_06
ORD IDord-025bb99909744c68b7fab9537bd0e935
出典メモuspto-grants-2012_06