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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280228Generated: October 29, 2026

Water → 5-[2-(p-[Ethoxycarbonylmethoxy]phenyl)ethen-1-yl]imidazo[1,5-a]pyridine

https://huagongshe.com/reaction/280228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant5-[2-(p-Hydroxyphenyl)ethen-1-yl]imidazo[1,5-a]pyridineHCID 54058527—
SolventDimethylformamideHCID 6228—
Product5-[2-(p-[Ethoxycarbonylmethoxy]phenyl)ethen-1-yl]imidazo[1,5-a]pyridineHCID 53874958—

Reaction Steps

A solution of 5-[2-(p-hydroxyphenyl)ethen-1-yl]imidazo[1,5-a]pyridine (2.36 g) in 10 ml of dimethylformamide is added to a slurry of 0.5 g of sodium hydride in 30 ml of dry dimethylformamide at 0° under nitrogen. After warming to room temperature ethyl bromoacetate (1.67 g) is added and the reaction is heated to 60° for 5 hours. Water (200 ml) is added and the solution is extracted with ethyl acetate. The combined organic phases are washed with water, dried over sodium sulfate and evaporated to yield 5-[2-(p-[ethoxycarbonylmethoxy]phenyl)ethen-1-yl]imidazo[1,5-a]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04588732
Source datasetuspto-grants-1986_05
ORD IDord-c6101cfb69cd4263aba46af87fd668f3
Source noteuspto-grants-1986_05