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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantCyanoacetic acidHCID 9740—
ReactantPhosphorus trichlorideHCID 24387—
Reactant5-(p-Aminophenyl)-1-(p-fluorophenyl)-1H-1,2,4-triazoleHCID 12676670—
SolventTriethylamineHCID 8471—
Product2-Cyano-4'-[1-(p-fluorophenyl)-1H-1,3,4-triazol-5-yl]acetanilideHCID 23469721—

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259504
Source datasetuspto-grants-1981_03
ORD IDord-db3e86551d084302be386692d5d23beb
Source noteuspto-grants-1981_03