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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775286Generated: November 1, 2026

6-Bromo-5-methyl-2-trifluoromethyl-2,3-dihydroimidazo [1,2-a]pyridin-2-ol hydrobromide → 6-Bromo-5-methyl-2-trifluoromethylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1775286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-5-methyl-2-trifluoromethyl-2,3-dihydroimidazo [1,2-a]pyridin-2-ol hydrobromideHCID 118035112—
SolventEthanolHCID 702—
Product6-Bromo-5-methyl-2-trifluoromethylimidazo[1,2-a]pyridineHCID 115403721112%

Reaction Steps

A mixture of 3.29 g of 6-bromo-5-methyl-2-trifluoromethyl-2,3-dihydroimidazo[1,2-a]pyridin-2-ol hydrobromide and 10 ml of ethanol was stirred under heat-reflux for 3 hours. The cooled reaction mixture was concentrated under reduced pressure, then water was added, and the mixture was extracted with ethyl acetate. The mixture was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain 2.72 g of 6-bromo-5-methyl-2-trifluoromethylimidazo[1,2-a]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260436B2
Source datasetuspto-grants-2016_02
ORD IDord-7554272c11ed4268a1a006d1b864c104
Source noteuspto-grants-2016_02