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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255282Generated: November 1, 2026

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

https://huagongshe.com/reaction/1255282

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 numberUS08455483B2
Source datasetuspto-grants-2013_06
ORD IDord-43c812308c3f45adb8a709ce2f8fd419
Source noteuspto-grants-2013_06