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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334512Generated: October 25, 2026

Phosphorus oxychloride → 2-(Chloromethyl)-5-(4-chlorophenyl)-1,3,4-oxadiazole

https://huagongshe.com/reaction/334512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-chloro-N'-(2-chloroacetyl)benzohydrazideHCID 521292—
SolventAcetonitrileHCID 6342—
Product2-(Chloromethyl)-5-(4-chlorophenyl)-1,3,4-oxadiazoleHCID 126824682%

Reaction Steps

To a mixture of 4-chlorobenzohydrazide 5 (1 g, 5.86 mmol) and K2CO3 (0.97 g, 7.03 mmol) in acetonitrile (30 mL) was added 2-chloroacetyl chloride (0.68 g, 6.08 mmol) dropwise at ambient temperature. The resulting mixture was stirred at ambient temperature for 16 hours. The solid was collected, washed with H2O and ether, and dried to afford 4-chloro-N′-(2-chloroacetyl)benzohydrazide 6 (1.2 g, 82%) which was used for the next step without further purification. A mixture of 4-chloro-N′-(2-chloroacetyl)benzohydrazide 6 (0.6 g, 2.43 mmol) and phosphorous oxychloride (0.37 g, 2.43 mmol) in acetonitrile (20 mL) was stirred under reflux for 16 hours and concentrated. The residue was subjected to flush column chromatography eluting with 10-25% acetone/hexanes to give compound 7 (0.45 g). Yield: 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883827B2
Source datasetuspto-grants-2014_11
ORD IDord-403a30879bc547fca00d9fe10fd8f003
Source noteuspto-grants-2014_11