Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085243Generated: October 30, 2026

Ethanol → 6-(4-Fluorophenyl)-2,3-dihydroimidazo[2,1-b][1,3]thiazole

https://huagongshe.com/reaction/1085243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4,5-Dihydro-2-thiazolamineHCID 15689—
Reactant2-Chloro-4'-fluoroacetophenoneHCID 120248—
SolventWaterHCID 962—
Product6-(4-Fluorophenyl)-2,3-dihydroimidazo[2,1-b][1,3]thiazoleHCID 1363989799%

Reaction Steps

A mixture of 51.6 g (0.3 mol) of 4-fluorophenacylchloride, 33.66 g (0.33 mol) of 2-aminothiazoline and 200 ml of ethanol was heated at reflux for 2 hours. The mixture was cooled to room temperature at which point 300 ml of water was added. After a reflux period of 2 hours, the mixture was concentrated to remove about 190 ml of aqueous alcohol. The pH of the residue was adjusted to about 2 with 10% hydrochloric acid (10 ml). The solid product was separated and dried to give 65.4 g (85%) of 6-(4-fluorophenyl)-2,3-dihydroimidazo[2,1-b]thiazole, m.p. 116-118°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008390
Source datasetuspto-grants-1991_04
ORD IDord-f58c4174469045b382dca4fb2bbeb62a
Source noteuspto-grants-1991_04