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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66013Generated: October 29, 2026

Acetonitrile → 1-benzyl-2,3-dihydro-1H-imidazo[1,2-a]pyridinium bromide

https://huagongshe.com/reaction/66013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantBenzyl BromideHCID 7498—
ReactantHCID 23423819HCID 23423819—
SolventDiethyl EtherHCID 3283—
Product1-benzyl-2,3-dihydro-1H-imidazo[1,2-a]pyridinium bromideHCID 86735012—

Reaction Steps

To 2.0 g. of 2,3-dihydroimidazo[1,2-a]pyridine in 40 ml. of dry acetonitrile is added 3.42 g. of α-bromotoluene and the resulting mixture heated to reflux overnight. The solution is cooled to room temperature and treated with 30 ml. of diethyl ether. The precipitated solid is filtered and recrystallized from acetonitrile, 1.64 g., m.p. 143°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04129567
Source datasetuspto-grants-1978_12
ORD IDord-f6469acff457428c8841e7511c65bfd0
Source noteuspto-grants-1978_12