HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334518Generated: October 29, 2026
Phosphorus oxychloride → 2-(Chloromethyl)-5-(3,4-dichlorophenyl)-1,3,4-oxadiazole
https://huagongshe.com/reaction/334518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3,4-dichloro-N'-(2-chloroacetyl)benzohydrazide | HCID 67479386 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(Chloromethyl)-5-(3,4-dichlorophenyl)-1,3,4-oxadiazole | HCID 2763466 | 78% |
Reaction Steps
To a mixture of 3,4-dichlorobenzohydrazide 8 (0.5 mg, 2.43 mmol) and K2CO3 (0.61 g, 4.4 mmol) in acetonitrile (30 mL) was added 2-chloroacetyl chloride (0.41 g, 3.66 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 3,4-dichloro-N′-(2-chloroacetyl)benzohydrazide 9 (0.59 g, 85%) which was used for the next step without further purification. A mixture of compound 9 (0.5.9 g, 2.24 mmol) and phosphorous oxychloride (0.51 g, 3.36 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 10 (0.43 g). Yield: 78%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883827B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-698e6c47b1b14be2a31ffc8cde13cc95 |
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| Source note | uspto-grants-2014_11 |
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