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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446406Generated: October 30, 2026

Imidazole → (2-(3-Bromobenzyloxy)ethoxy)(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/446406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-(3-Bromobenzyloxy)ethanolHCID 57956818—
SolventDichloromethaneHCID 6344—
Product(2-(3-Bromobenzyloxy)ethoxy)(tert-butyl)dimethylsilaneHCID 58168604—

Reaction Steps

A solution of 2-(3-bromobenzyloxy)ethanol [Aromatic Intermediate 25, step a] (3 g), imidazole (2.2 g) and tert-butyldimethylchlorosilane (2.2 g) in DCM (50 mL) was stirred at RT for 17 hours. The reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate (×2). The combined organic phases were dried and evaporated in vacuo. The crude product was purified by silica gel chromatography, gradient elution 10 to 40% ethyl acetate in isohexane. Fractions containing the product were evaporated to dryness to afford the subtitled compound as a colourless oil. Yield 3.8 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476265B2
Source datasetuspto-grants-2013_07
ORD IDord-b25c7bdaf16b407e9b20658b39f96864
Source noteuspto-grants-2013_07