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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606406Generated: October 25, 2026

Pyridine → N-(pentabromobenzoyl)-3,4-dibromohexahydrophthalimide

https://huagongshe.com/reaction/1606406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3,4-DibromohexahydrophthalimideHCID 21542796—
ReactantPentabromobenzoyl chlorideHCID 23051734—
SolventBenzeneHCID 241—
ProductN-(pentabromobenzoyl)-3,4-dibromohexahydrophthalimideHCID 21542799—

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. Pentabromobenzoyl 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-(pentabromobenzoyl)-3,4-dibromohexahydrophthalimide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953397
Source datasetuspto-grants-1976_04
ORD IDord-16fffd1a9f0242d4b94c5b7de4b2c59f
Source noteuspto-grants-1976_04