Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648883Generated: October 30, 2026

Pyridine → HCID 20144038, compound

https://huagongshe.com/reaction/648883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
Reactant4-Cyanobenzoyl chlorideHCID 80172—
Reactantα-PyridoinHCID 95624—
SolventAcetonitrileHCID 6342—
ProductHCID 20144038HCID 20144038—

Reaction Steps

To 2.14 g (0.01 mole) of α-pyridoin in 50 ml of acetonitrile was added 0.80 g (0.01 mole) of pyridine and then 1.65 g (0.01 mole) of p-cyanobenzoyl chloride portionwise with stirring. Stirring was continued for 1/2 hour. Then 150 ml of dichloromethane was added, the organic phase washed thoroughly with water, dried and evaporated to an oily solid residue. The residue was stirred with 80% hexane and 20% acetone to obtain a solid, 1.7 g (50%). After recrystallization from hexane-acetone, 0.9 g (53%), m.p., 152°-154° C., of NA-VI was recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04737439
Source datasetuspto-grants-1988_04
ORD IDord-56438169cbc84ff6ba4d7c1f315f0867
Source noteuspto-grants-1988_04