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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357008Generated: October 25, 2026

Water → 1-Butanol,4-(imidazo[1,2-a]pyridin-5-yloxy)-

https://huagongshe.com/reaction/357008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(Dimethyl-tert-butylsilyl)oxybutan-1-olHCID 186403—
Reactant5-Chloroimidazo[1,2-a]pyridine hydrochlorideHCID 21994174—
SolventDimethyl SulfoxideHCID 679—
Product1-Butanol,4-(imidazo[1,2-a]pyridin-5-yloxy)-HCID 18936813—

Reaction Steps

In a nitrogen stream, 8.0 g (200 mmol) of 60% oily sodium hydride was added to a solution of 18.90 g (100 mmol) of 5-chloroimidazo[1,2-a]pyridine hydrochloride in 200 ml of dimethyl sulfoxide at 0° C., followed by stirring for 15 minutes. To this mixture, 20.44 g (100 mmol) of 4-hydroxy-1-t-butyldimethylsiloxybutane was added, followed by stirring room temperature for 5 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to yield 3.73 g (11.6%, orange oily substance) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-3dc2156c8ccc40a8a198198e69ef81ad
Source noteuspto-grants-1998_11