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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177047Generated: October 31, 2026

Imidazole → 2-(Tert-butyldimethylsilyl)oxy-1-phenylethanol

https://huagongshe.com/reaction/2177047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant1-Phenyl-1,2-ethanediolHCID 7149—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDichloromethaneHCID 6344—
Product2-(Tert-butyldimethylsilyl)oxy-1-phenylethanolHCID 1139111698.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) and stirred solution of 1-phenylethane-1,2-diol (1.0 g, 7.24 mmol) and tert-butyldimethylsilyl chloride (1.1 g, 7.24 mmol) in dichloromethane was added imidazole (0.74 g, 10.86 mmol). The reaction mixture was slowly warmed to room temperature and stirred for 20 hours. The reaction mixture was washed with water, dried, and concentrated to yield 1.8 g of 2-(tert-butyldimethylsilanyloxy)-1-phenylethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067897B2
Source datasetuspto-grants-2015_06
ORD IDord-764039ffac994cc1a23e77f7ba38a673
Source noteuspto-grants-2015_06