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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977660Generated: October 30, 2026

Imidazole → Benzyl({2-[(tert-butyldimethylsilyl)oxy]ethyl})amine

https://huagongshe.com/reaction/1977660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-Benzyl-aminoethanolHCID 18380309—
SolventWaterHCID 962—
ProductBenzyl({2-[(tert-butyldimethylsilyl)oxy]ethyl})amineHCID 21993563—

Reaction Steps

An N,N-dimethylformamide (40 ml) solution of 2-benzyl-aminoethanol (3 g), tert-butyldimethylsilyl chloride (3.6 g), and imidazole (3.4 g) was stirred at room temperature for 1 hour in a stream of argon air. Water (300 ml) was added to the reaction solution, and the solution was extracted with ethyl acetate. The organic phase was washed with water and saturated brine, dried over sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was dried to obtain the desired compound (5.3 g, quantitative) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235730B1
Source datasetuspto-grants-2001_05
ORD IDord-bdb7e3eb936c453ca39016c012005e8d
Source noteuspto-grants-2001_05