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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606404Generated: October 25, 2026

Pyridine → N-(2,4,6-tribromobenzoyl)-3,4-dibromohexahydrophthalimide

https://huagongshe.com/reaction/1606404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,4,6-tribromobenzoyl ChlorideHCID 11234266—
Reactant3,4-DibromohexahydrophthalimideHCID 21542796—
SolventBenzeneHCID 241—
ProductN-(2,4,6-tribromobenzoyl)-3,4-dibromohexahydrophthalimideHCID 21542800—

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. 2,4,6-Tribromobenzoyl 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 ans stripped of solvent under reduced pressure to yield the desired product N-(2,4,6-tribromobenzoyl)-3,4-dibromohexahydrophthalimide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953397
Source datasetuspto-grants-1976_04
ORD IDord-f33b8bfbee8b4bce8cc143e67b2fe5ac
Source noteuspto-grants-1976_04