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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745418Generated: November 2, 2026

Pyridine → HCID 22226281, compound

https://huagongshe.com/reaction/1745418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 53675890HCID 53675890—
SolventEthanolHCID 702—
ProductHCID 22226281HCID 22226281—

Reaction Steps

2.4 g of 1-bromomethylcyclopropylketone and 5.8 cm3 of pyridine are introduced into a three-necked flask containing 40 cm3 of ethanol and then the mixture is heated for 2 hours under reflux. After concentrating to dryness at 40° C. under reduced pressure (2.7 kPa), the residue is taken up in twice 30 cm3 of diethyl. ether. After filtration, washing with diethyl ether, the precipitate is dried under reduced pressure (90 Pa) to give 3.4 g of 1-cyclopropylcarbonylmethylpyridinium bromide in the form of a cream-coloured solid melting at 160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019110B2
Source datasetuspto-grants-2006_03
ORD IDord-711ededf458c4691a77b233758e28a62
Source noteuspto-grants-2006_03