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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625906Generated: October 26, 2026

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

https://huagongshe.com/reaction/1625906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(5-Bromo-2-chlorophenyl)methanolHCID 5074766—
SolventDimethylformamideHCID 6228—
Product(5-Bromo-2-chlorobenzyloxy)(tert-butyl)diphenylsilaneHCID 57516661—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-c3c319d56e834468b57611e9a074b802
Source noteuspto-grants-2014_07