HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128460Generated: October 30, 2026
Acetonitrile → 2-Cyano-4'-[1-(p-fluorophenyl)-1H-1,3,4-triazol-5-yl]acetanilide
https://huagongshe.com/reaction/128460
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | 5-(p-Aminophenyl)-1-(p-fluorophenyl)-1H-1,2,4-triazole | HCID 12676670 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-Cyano-4'-[1-(p-fluorophenyl)-1H-1,3,4-triazol-5-yl]acetanilide | HCID 23469721 | — |
Reaction Steps
A solution of 3.5 ml. of phosphorus trichloride in 25 ml. of acetonitrile is added dropwise to a stirred suspension of 19.0 g. of 5-(p-aminophenyl)-1-(p-fluorophenyl)-1H-1,2,4-triazole in a mixture of 15.6 ml. of triethylamine, 6.35 g. of cyanoacetic acid and 200 ml. of acetonitrile at room temperature over a period of one hour. The mixture is heated to boiling, giving a clear solution and kept at 90° C. for 2.5 hours. The suspension is filtered hot through diatomaceous earth. The filtrate is heated to boiling, 250 ml. of hot water is added and the solution is slowly cooled to 5° C. A 400 ml. portion of water is added and the solid is collected and recrystallized from ethanol giving the desired product as 19.0 g. of cream crystals, mp. 223°-225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04259504 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-db3e86551d084302be386692d5d23beb |
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| Source note | uspto-grants-1981_03 |
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