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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196441Generated: October 31, 2026

Imidazole → (2-Bromobenzyloxy)tert-butyldimethylsilane

https://huagongshe.com/reaction/2196441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant2-Bromobenzyl alcoholHCID 72850—
ReactantTert-butyldimethylsilane chlorideHCID 131722836—
SolventTetrahydrofuranHCID 8028—
Product(2-Bromobenzyloxy)tert-butyldimethylsilaneHCID 1342490082.6%

Reaction Steps

2.0 g of (2-bromophenyl)methanol are placed in a round-bottomed flask and dissolved in 100 ml of tetrahydrofuran. 1.1 g of 1H-imidazole are added thereto, followed by 2.1 g of tert-butyldimethylsilane chloride, and the mixture is left to stir at ambient temperature for 48 hours. The reaction mixture is then hydrolysed with water, and the organic phase, which has been extracted with ethyl acetate, is separated, dried over magnesium sulphate and concentrated under reduced pressure. The residue obtained is purified by silica gel chromatography, elution being carried out with a heptane/ethyl acetate mixture. 2.66 g of compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338451B2
Source datasetuspto-grants-2012_12
ORD IDord-31c87749347749b681e3724889802906
Source noteuspto-grants-2012_12