HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334516Generated: October 29, 2026
Chloroacetyl chloride → HCID 13365860, compound
https://huagongshe.com/reaction/334516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-dichlorobenzohydrazide | HCID 2735966 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13365860 | HCID 13365860 | 93.2% |
Reaction Steps
To a mixture of 3,5-dichlorobenzohydrazide 5 (0.5 g, 2.4 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 3,5-dichloro-N′-(2-chloroacetyl)benzohydrazide 6 (0.63 g, 92%) which was used for the next step without further purification. A mixture of 3,5-dichloro-N′-(2-chloroacetyl)benzohydrazide 6 (0.63 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 7 (0.52 g). Yield: 88%.
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-bb364b2401db429ab2e07ea7f6e7689b |
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| Source note | uspto-grants-2014_11 |
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