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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077292Generated: November 3, 2026

Triethylamine → HCID 21536164, compound

https://huagongshe.com/reaction/1077292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,6-Difluorobenzoyl chlorideHCID 87438—
ReactantHCID 21536153HCID 21536153—
SolventTolueneHCID 1140—
ProductHCID 21536164HCID 21536164—

Reaction Steps

2-(4-Fluorophenyl)-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-(4-fluorophenyl)-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-2238c2dfc45d4518a42ef1d959cd0222
Source noteuspto-grants-1976_05