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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077293Generated: October 29, 2026

Triethylamine → HCID 21536163, compound

https://huagongshe.com/reaction/1077293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,6-Difluorobenzoyl chlorideHCID 87438—
ReactantHCID 21536150HCID 21536150—
SolventTolueneHCID 1140—
ProductHCID 21536163HCID 21536163—

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-Difluorobenzoyl 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-difluorobenzoyl)-1,2,4-oxadiazolidin-3,5-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959478
Source datasetuspto-grants-1976_05
ORD IDord-44b887af641c4938bfc2c2108e302a72
Source noteuspto-grants-1976_05