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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516892Generated: October 29, 2026

Imidazole → Benzyl 3-(4-((tert-butyldimethylsilyl)oxy)phenyl)propanoate

https://huagongshe.com/reaction/516892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantBenzyl 3-(4-hydroxyphenyl)propanoateHCID 14211262—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-(4-((tert-butyldimethylsilyl)oxy)phenyl)propanoateHCID 5970650195%

Reaction Steps

A solution of benzyl 3-(4-hydroxyphenyl)propanoate (1.0 g, 11.70 mmol) in dichloromethane (60 ml) was cooled to 0° C., and imidazole (1.30 g, 18.73 mmol) and tert-butylchlorodimethylsilane (1.94 g, 12.87 mmol) were added thereto, and the mixture was stirred at room temperature for 15 hr. The reaction mixture was diluted with water and was extracted with ethyl acetate. The organic layer was washed with saturated brine and was dried over anhydrous sodium sulfate, and the filtrate was removed by distillation under reduced pressure. The residue was chromatographed on silica gel column (hexane:ethyl acetate=95:5) to give the title compound as an oil (4.0 g, yield 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115079B2
Source datasetuspto-grants-2015_08
ORD IDord-574aeabcf769446d9e3457bf64a55302
Source noteuspto-grants-2015_08