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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606396Generated: October 26, 2026

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

https://huagongshe.com/reaction/1606396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,3,5-Trichlorobenzoyl chlorideHCID 13011116—
Reactant3,4-DibromohexahydrophthalimideHCID 21542796—
SolventBenzeneHCID 241—
ProductN-(2,3,5-trichlorobenzoyl)-3,4-dibromohexahydrophthalimideHCID 21542804—

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. 2,3,5-Trichlorobenzoyl 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-(2,3,5-trichlorobenzoyl)-3,4-dibromohexahydrophthalimide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953397
Source datasetuspto-grants-1976_04
ORD IDord-b3d93a2c772643efab1aadf176995c34
Source noteuspto-grants-1976_04