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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376618Generated: November 1, 2026

Water → 5-Acetoxymethylimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1376618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
Reactant5-Hydroxymethylimidazo[5,1-b]thiazoleHCID 18359987—
SolventDichloromethaneHCID 6344—
Product5-Acetoxymethylimidazo[5,1-b]thiazoleHCID 2291666581%

Reaction Steps

To a solution of 0.231 g (1.50 mmol) of the 5-Hydroxymethylimidazo[5,1-b]thiazole prepared in Preparation 10 in 8 ml of dichloromethane was added 0.156 ml (1.65 mmol) of acetic anhydride with ice-cooling, and the mixture was stirred at room temperature for 20 hours. To the reaction solution were added water and a saturated aqueous solution of sodium hydrogencarbonate, and the mixture was extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, and concentrated to dryness under reduced pressure. The residue was purified by flash column chromatography using silica gel, eluting with a 30:1 mixture of chloroform and methanol to give 0.237 g (yield 81%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663162
Source datasetuspto-grants-1997_09
ORD IDord-3c2750eb28de434c97b5a8906f065299
Source noteuspto-grants-1997_09