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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757437Generated: November 2, 2026

Imidazole → 1-Bromo-3-((((1,1-dimethylethyl)dimethylsilyl)oxy)methyl)benzene

https://huagongshe.com/reaction/1757437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-Bromobenzyl alcoholHCID 85141—
SolventDichloromethaneHCID 6344—
Product1-Bromo-3-((((1,1-dimethylethyl)dimethylsilyl)oxy)methyl)benzeneHCID 2203314798.2%

Reaction Steps

To a solution of 3-bromobenzyl alcohol (5.00 g, 26.7 mmol) in freshly drieddimethylformamide (10 mL) was added t-butyldimethylsilyl chloride (5.13 g, 33 mmol) and imidazole (4.56 g, 67 mmol). The resulting solution was stirred overnight at ambient temperature. The reaction mixture was poured into water and extracted (3x, 50 mL 1:1 ether:hexanes). The combined organic layers were washed (2x, brine), dried over MgSO4, filtered, and concentrated in vacuo to give a colorless oil which was passed througha short silica gel plug using 10% methylene chloride:hexanes to give pure 3-(t-butyldimethylsilyloxymethyl)bromobenzene (7.9 g, 98%). 1H NMR (300 MHz, CDCl3) δ 7.47 (1H, br s), 7.37 (1H, dt, J =7, 1 Hz), 7.16-7.25 (2H, m), 4.24 (2H, s), 0.94 (9H, s), 0.11 (6H, s). MS m/e 318/320(M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446055
Source datasetuspto-grants-1995_08
ORD IDord-94cfe40066b04d62a44ba142a762167a
Source noteuspto-grants-1995_08