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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891624Generated: October 31, 2026

Ethanol → [2-(t-Butyldiphenylsilyloxy)ethyl]carbamic acid benzyl ester

https://huagongshe.com/reaction/891624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactantbenzyl N-(2-hydroxyethyl)carbamateHCID 280458—
SolventDimethylformamideHCID 6228—
Product[2-(t-Butyldiphenylsilyloxy)ethyl]carbamic acid benzyl esterHCID 16221537100%

Reaction Steps

Subsequently, to a solution of (2-hydroxyethyl)carbamic acid benzyl ester (5.37 g, 27.5 mmol) in dimethylformamide (160 ml) were added t-butyldiphenylsilyl chloride (8.6 ml, 33.0 mmol) and imidazole (2.3 g, 33.8 mmol) in an ice bath, and the mixture was stirred at room temperature overnight. After checking the completion of the reaction, ethanol was added thereto and the reaction mixture was stirred for 2 hours. The reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using hexane:ethyl acetate (5:1) as the eluant to afford [2-(t-butyldiphenylsilyloxy)ethyl]carbamic acid benzyl ester (11.93 g, yield 100%) as a colorless and transparent syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-9b693292ca47482682ecf12204b04792
Source noteuspto-grants-2006_02