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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651241Generated: October 29, 2026

2-Chloroacrylonitrile → 4-Cyano-1-(2,6-difluorobenzyl)-1H-1,2,3-triazole

https://huagongshe.com/reaction/651241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroacrylonitrileHCID 70198—
Reactant2-(Azidomethyl)-1,3-difluorobenzeneHCID 10888323—
SolventHeptaneHCID 8900—
Product4-Cyano-1-(2,6-difluorobenzyl)-1H-1,2,3-triazoleHCID 11042239—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2,6-difluorobenzyl azide (34.2 g) and 2-chloroacrylonitrile (26.6 g) is stirred at about 80° C. for 24 hours. n-Heptane (125 ml) is allowed to run in, and unreacted 2chloroacrylonitrile and 2,6-difluorobenzyl azide as well as n-heptane are distilled off (distillate 50 ml) by raising the external temperature to about 130° C. The mixture is cooled to about 20° C. and the suspension is stirred at about 20° C. for 1 hour. The product is isolated by filtration and washed with n-heptane (100 ml). The product is dried in vacuo at about 60° C. Yield: 31.55 g=71.6% (beige powder).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277999B1
Source datasetuspto-grants-2001_08
ORD IDord-f6bf64ebbfa2440e8c3892790d99f3ec
Source noteuspto-grants-2001_08