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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481025Generated: October 31, 2026

Benzyl Alcohol → 8-(Benzyloxy)-6-bromo-2,3-dimethylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/481025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
Reactant6,8-Dibromo-2,3-dimethylimidazo[1,2-a]pyridineHCID 12106080—
SolventDimethylformamideHCID 6228—
Product8-(Benzyloxy)-6-bromo-2,3-dimethylimidazo[1,2-a]pyridineHCID 12106081—

Reaction Steps

34.8 ml of benzyl alcohol are added dropwise with ice-cooling to a suspension of 13.5 g of sodium hydride (60% strength suspension in paraffin) in 510 ml of dimethylformamide and the mixture is stirred for 1 h until the evolution of gas is complete. 51.2 g of 6,8-dibromo-2,3-dimethylimidazo[1,2-a]pyridine are then introduced in small portions and the mixture is stirred at room temperature for 40 h. It is then poured onto 1 l of ice water, extracted three times with 100 ml of dichloromethane each time, the combined organic extracts are washed with saturated aqueous ammonium chloride solution and twice with water and concentrated to dryness in vacuo, and the residue is stirred with a little ethyl acetate. The precipitate obtained here is filtered off and dried in vacuo. 43.2 g of the title compound of melting point 151-3° C. (ethyl acetate) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653477B2
Source datasetuspto-grants-2003_11
ORD IDord-373a725b972848e592af8194c0355b46
Source noteuspto-grants-2003_11