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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334515Generated: October 27, 2026

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

https://huagongshe.com/reaction/334515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN'-(2-chloroacetyl)-4-methylbenzohydrazideHCID 736971—
SolventAcetonitrileHCID 6342—
Product2-(Chloromethyl)-5-(4-methylphenyl)-1,3,4-oxadiazoleHCID 73697372.4%

Reaction Steps

To a mixture of 4-methylbenzohydrazide 14 (10 g, 66.59 mmol) and K2CO3 (16.57 g, 119.86 mmol) in acetonitrile (100 mL) was added 2-chloroacetyl chloride (9.02 g, 79.9 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 N′-(2-chloroacetyl)-4-methylbenzohydrazide 15 (13 g, 82%) which was used for the next step without further purification. A mixture of N′-(2-chloroacetyl)-4-methylbenzohydrazide 15 (6.0 g, 26.47 mmol) and phosphorous oxychloride (5.0 g, 32.84 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 16 (4 g). Yield: 72%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883827B2
Source datasetuspto-grants-2014_11
ORD IDord-d8cef926cf654c9f9a0f2e30b686da86
Source noteuspto-grants-2014_11