Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364469Generated: October 31, 2026

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

https://huagongshe.com/reaction/1364469

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 numberUS07888366B2
Source datasetuspto-grants-2011_02
ORD IDord-44b8dde966ec42caaed58997931514a5
Source noteuspto-grants-2011_02