Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483348Generated: October 30, 2026

2-Chloro-5-(chloromethyl)pyridine → 2-[(6-Chloropyridin-3-yl)methyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/483348

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-(chloromethyl)pyridineHCID 155479—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDichloromethaneHCID 6344—
Product2-[(6-Chloropyridin-3-yl)methyl]-1H-isoindole-1,3(2H)-dioneHCID 14324713—

Reaction Conditions

Temperature160 °C

Reaction Steps

2-Chloro-5-chloromethylpyridine (8.1 g, 0.05 mol) and potassium phthalimide (10.2 g, 0.055 mol) were mixed together at ambient temperature (20° C.) and the resulting mixture was then heated with stirring at 160° C. for 12 hours. The reaction mixture was then cooled to ambient temperature (20° C.) and dichloromethane was added until most of the solid residue had dissolved. The dichloromethane extract was then washed with water (2×150 ml) and brine (1×200 ml), dried using magnesium sulphate, and evaporated under reduced pressure to give a light-brown solid. The title product, N-(6-chloro-3-pyridylmethyl) phthalimide, was isolated from this solid by flash chromatography using silica gel, 230 to 400 US mesh (0.062 mm to 0.037 mm), with 10% v/v ether/ dichloromethane as eluent, as a buff solid (10.70 g, 78.5%), mp 140° to 142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225423
Source datasetuspto-grants-1993_07
ORD IDord-7302564473bf4a568aabbd8983a67672
Source noteuspto-grants-1993_07