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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068230Generated: November 2, 2026

Bromine → 3-Bromo-2-ethyl-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1068230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant2-Ethylimidazo[1,2-a]pyridineHCID 21831991—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-Bromo-2-ethyl-imidazo[1,2-a]pyridineHCID 2191274166.8%

Reaction Steps

To a solution of 2-ethyl-imidazo[1,2-a]pyridine (2.17 g, 14.9 mmol) in EtOH (25 mL) was added Br2 (2.0 g, 12.5 mmol) in H2O (5 mL) dropwise at rt. After stirring at rt for 4 h, EtOH was evaporated under reduced pressure. The residue was basified with aqueous NaHCO3 and extracted with CH2Cl2 (3×). The organic phase was washed with brine and dried over anhydrous MgSO4. Concentration followed by flash chromatography chromatography eluting with 20% EtOAc in hexanes, followed by 50% EtOAc in hexanes afforded the title compound (1.88 g) as a viscous oil. 1H NMR (500 MHz, CDCl3): δ 1.36 (t, J=7.5 Hz, 3H), 2.83 (q, J=7.6 Hz, 2H), 6.88 (t, J=6.8 Hz, 1H), 7.20 (m, 1H), 7.55 (dd, J=8.9, 0.9 Hz, 1H), 8.05 (dd, J=6.9, 1.2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248755B1
Source datasetuspto-grants-2001_06
ORD IDord-a6e03872aea24589a3d57b706e9c1a4f
Source noteuspto-grants-2001_06