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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606401Generated: October 31, 2026

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

https://huagongshe.com/reaction/1606401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,5-Dibromobenzoyl chlorideHCID 13450524—
Reactant3,4-DibromohexahydrophthalimideHCID 21542796—
SolventBenzeneHCID 241—
ProductN-(2,5-dibromobenzoyl)-3,4-dibromohexahydrophthalimideHCID 21542806—

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. 2,5-Dibromobenzoyl 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-(2,5-dibromobenzoyl)-3,4-dibromohexahydrophthalimide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953397
Source datasetuspto-grants-1976_04
ORD IDord-838fdf3f81364b2abd22222530d83333
Source noteuspto-grants-1976_04