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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709777Generated: November 1, 2026

Imidazole → 3-(Benzyloxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-chloropyridine

https://huagongshe.com/reaction/709777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(5-(Benzyloxy)-6-chloropyridin-3-yl)methanolHCID 117760270—
SolventDimethylformamideHCID 6228—
Product3-(Benzyloxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-chloropyridineHCID 131733915102.9%

Reaction Steps

To a solution of (5-(benzyloxy)-6-chloropyridin-3-yl)methanol (1.76 g) and tert-butyldimethylchlorosilane (1.59 g) in DMF (10 mL) was added imidazole (960 mg), and the mixture was stirred at room temperature for 14 hr. Water was added to the reaction mixture at room temperature, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.64 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-6604187d3659418d81865fd301b616f3
Source noteuspto-grants-2015_11