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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603492Generated: November 2, 2026

Allyl Alcohol → 3-(Allyloxycarbonyl)methylimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1603492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantSodium ethoxideHCID 2723922—
Reactant3-Ethoxycarbonylmethylimidazo[5,1-b]thiazoleHCID 19605065—
Product3-(Allyloxycarbonyl)methylimidazo[5,1-b]thiazoleHCID 19605012—

Reaction Steps

A 30 mg potion of a sodium ethoxide powder was added to 6.2 ml of an allyl alcohol solution containing 314.2 mg of 3-ethoxycarbonylmethylimidazo[5,1-b]thiazole, and the mixture was then was then heated under reflux for 7 hours. After cooled, the reaction solution was concentrated under reduced pressure, and the organic layer extracted with dichloromethane (10 ml×4) was dried over anhydrous magnesium sulfate, and then filtered, and the solvent was evaporated under reduced pressure. The resulting crude product was purified by a silica gel column chromatograph to obtain 240.4 mg of the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990101
Source datasetuspto-grants-1999_11
ORD IDord-bcc09a9dffdc4d64a4f4c2988d62cb07
Source noteuspto-grants-1999_11