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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077286Generated: October 30, 2026

Triethylamine → HCID 21536162, compound

https://huagongshe.com/reaction/1077286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
ReactantHCID 21536150HCID 21536150—
SolventTolueneHCID 1140—
ProductHCID 21536162HCID 21536162—

Reaction Steps

2-(3-Chlorophenyl)-1,2,4-oxadiazolidin-3,5-dione (0.03 mole), toluene (100 ml) and triethylamine (5 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2,6-Dichlorobenzoyl chloride (0.03 mole) dissolved in toluene (20 ml) is then added to the reaction flask and the resulting mixture is heated at reflux with stirring for a period of about 24 hours. After this time the reaction mixture is filtered and the filtrate is washed with water, dilute hydrochloric acid and with aqueous sodium bicarbonate. The washed solution is then dried over anhydrous magnesium sulfate. The dried solution is stripped of solvent under reduced pressure leaving a solid residue. The residue is recrystallized to yield the desired product 2-(3-chlorophenyl)-4-(2,6-dichlorobenzoyl)-1,2,4-oxadiazolidin-3,5-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959478
Source datasetuspto-grants-1976_05
ORD IDord-9ed923f291a146a3b1308270ef499ead
Source noteuspto-grants-1976_05