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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396437Generated: October 30, 2026

Hydrochloric Acid → 1-(4-Chloro-pyridin-2-yl)-ethanone

https://huagongshe.com/reaction/396437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-2-pyridinecarbonitrileHCID 693342—
ReactantHCID 178418373HCID 178418373—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Product1-(4-Chloro-pyridin-2-yl)-ethanoneHCID 1301198660%

Reaction Steps

To a solution of 4-chloro-2-pyridinecarbonitrile (5.35 g, 38.6 mmol) in benzene (50 ml) and ether (50 ml) cooled to 0° C. was added dropwise over 20 min a 2M solution of MeMgI in ether (23 ml, 46.3 mmol). After 0.5 h, the mixture was allowed to warm to ambient temperature, and stirring continued for 2 h. The mixture was cooled to 0° C. and 2M aqueous HCl (100 ml) added. The mixture was made basic with saturated aqueous sodium bicarbonate (˜80 ml) and the organic layer separated and dried (MgSO4). After removal of solvent, the residue was purified by flash chromatography eluting with ethyl acetate/hexane (1:5) to afford 3.60 g (60%) of 2-acetyl-4-chloropyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608070B1
Source datasetuspto-grants-2003_08
ORD IDord-54c5df0661cf42e9a2f0b76b507c5e8c
Source noteuspto-grants-2003_08