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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606399Generated: October 25, 2026

Pyridine → N-(2,3,4,5-tetrachlorobenzoyl)-3,4-dibromohexahydrophthalimide

https://huagongshe.com/reaction/1606399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,3,4,5-Tetrachlorobenzoyl chlorideHCID 5463797—
Reactant3,4-DibromohexahydrophthalimideHCID 21542796—
SolventBenzeneHCID 241—
ProductN-(2,3,4,5-tetrachlorobenzoyl)-3,4-dibromohexahydrophthalimideHCID 21542798—

Reaction Steps

3,4-Dibromohexahydrophthalimide (0.10 mole), benzene (300 ml) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2,3,4,5-Tetrachlorobenzoyl chloride (0.10 mole) is then added dropwise to the flask with stirring at room temperature. After the addition is completed the reaction mixture is heated at reflux with continued stirring for a period of about 1 hour. After this time the reaction mixture is filtered and the filtrate is washed with water. The washed filtrate is then dried over anhydrous magnesium sulfate, filtered and stripped of solvent under reduced pressure to yield the desired product N-(2,3,4,5-tetrachlorobenzoyl)-3,4-dibromohexahydrophthalimide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953397
Source datasetuspto-grants-1976_04
ORD IDord-1e165ab5283d46c68ff97a4e46c7baa8
Source noteuspto-grants-1976_04