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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973672Generated: October 29, 2026

Water → 1,3,4-Oxadiazol-2(3H)-one, 5-(4-chlorophenyl)-

https://huagongshe.com/reaction/973672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexaneHCID 8058—
ReactantDiphosgeneHCID 10426—
Reactant4-ChlorobenzohydrazideHCID 10816—
SolventDichloromethaneHCID 6344—
Product1,3,4-Oxadiazol-2(3H)-one, 5-(4-chlorophenyl)-HCID 1111698293.3%

Reaction Steps

To a suspension of 4-chlorobenzhydrazide (8.53 grams (g), 0.05 mole) in methylene chloride (100 milliliters (ml)), was dropwise added trichloromethyl chloroformate (5.94 g, 0.03 mole). After addition, the reaction mixture was heated to reflux for 2 hours. The reaction was cooled down to room temperature and poured into a mixture of water (500 ml) and hexane (200 ml) and stirred for 10 to 20 min. The resultant precipitate was collected by suction-filtration and was washed with hexane to give a solid product. The product was dried in air at room temperature overnight yielding 5.5 g (60% yield) of 2-(4-chlorophenyl)-1,3,4-oxadiazolin-5one as a solid, m.p. 225°-227° C. NMR and IR spectra showed the desired structure. Without further purification, this product was subjected to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05064845
Source datasetuspto-grants-1991_11
ORD IDord-a31978202d9f45f4b7d7740f8b440bc0
Source noteuspto-grants-1991_11