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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521686Generated: October 31, 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/521686

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 numberUS09328121B1
Source datasetuspto-grants-2016_05
ORD IDord-94deecfee1c445ada316de5ed67e045c
Source noteuspto-grants-2016_05