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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616326Generated: November 3, 2026

Thionyl Chloride → HCID 20369656, compound

https://huagongshe.com/reaction/616326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 20369676HCID 20369676—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 20369656HCID 20369656—

Reaction Steps

2-(3,4-Dichlorophenyl)-4-hydroxymethyl-1,2,4-oxadiazolidin-3,5-dione (0.03 mole) dissolved in chloroform (40 ml) and thionyl chloride (0.06 mole) dissolved in chloroform (10 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux for a period of about 2 hours. After this time the reaction mixture is stripped of solvent under reduced pressure, leaving a residue. This residue is dissolved in toluene, and the toluene solution is stripped of solvent and unreacted starting materials to yield the desired product 2-(3,4-dichloropheny)-4-chloromethyl-1,2,4-oxadiazolidin-3,5-dione as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04073894
Source datasetuspto-grants-1978_02
ORD IDord-2d299aa4c36c426a83ea63d04f421f12
Source noteuspto-grants-1978_02