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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043655Generated: November 1, 2026

4-Fluorophenol → 2-(4-Fluoro-phenoxy)-imidazo[2,1-b][1,3,4]thiadiazole

https://huagongshe.com/reaction/1043655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
Reactant2-Bromoimidazo[2,1-b][1,3,4]thiadiazoleHCID 43667923—
SolventDichloromethaneHCID 6344—
Product2-(4-Fluoro-phenoxy)-imidazo[2,1-b][1,3,4]thiadiazoleHCID 6733611653%

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 2-bromo-imidazo[2,1-b][1,3,4]thiadiazole (1.0 g, 4.90 mmol) and 4-fluorophenol (2.2 g, 19.60 mmol) was heated under microwave irradiation at 135° C. for 3.5 hours. On cooling, the mixture was diluted with dichloromethane (7 mL), adsorbed in silica and purified by column chromatography (Biotage™/Flash, silica, methanol:dichloromethane 0.2:9.8 to 2:8) to give 2-(4-fluoro-phenoxy)-imidazo[2,1-b][1,3,4]thiadiazole as a white solid (610 mg, 53% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563550B2
Source datasetuspto-grants-2013_10
ORD IDord-0cd89577a83c46468ccde53d20b1a5b6
Source noteuspto-grants-2013_10