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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457728Generated: October 30, 2026

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

https://huagongshe.com/reaction/457728

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 and extracted three times with 100 ml of dichloromethane each time. The combined organic extracts are washed with saturated 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 numberUS07189736B2
Source datasetuspto-grants-2007_03
ORD IDord-f8f7a82d4ebc43b982eb415e826c1af2
Source noteuspto-grants-2007_03