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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252348Generated: October 31, 2026

Hydrochloric Acid → 7-Bromo-1-(3-methoxypropenyl)imidazo[1,5-a]pyridine

https://huagongshe.com/reaction/252348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant(2-Methoxy-ethyl)-triphenyl-phosphonium, bromideHCID 22377376—
Reactant7-Bromoimidazo[1,5-a]pyridine-1-carbaldehydeHCID 83839570—
SolventDimethylformamideHCID 6228—
Product7-Bromo-1-(3-methoxypropenyl)imidazo[1,5-a]pyridineHCID 66888848—

Reaction Steps

A suspension of 12.04 g of (2-methoxyethyl)triphenylphosphonium bromide [55894-16-1] in 50 ml of anhydrous N,N-dimethylformamide is admixed with 2.60 g of sodium hydride (60% dispersion). The reaction mixture is stirred at room temperature for 30 minutes and a solution of 6.75 g of 7-bromoimidazo[1,5-a]pyridine-1-carbaldehyde in 20 ml of N,N-dimethylformamide is added. The reaction mixture is subsequently stirred at 50° C. for 1 hour. The reaction mixture is cooled to room temperature and poured onto ice-water. The quenched mixture is acidified with 1M HCl and extracted with tert-butyl methyl ether (3×100 ml). The combined organic phases are washed with water (100 ml) and brine (100 ml), dried over sodium sulphate and concentrated by evaporation. The title compound is identified on the basis of the Rf value from the residue by means of flash chromatography (SiO2 60F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868036B2
Source datasetuspto-grants-2011_01
ORD IDord-150386dfa9b24d6296fe18b05c093250
Source noteuspto-grants-2011_01