HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651242Generated: October 30, 2026
2-Chloroacrylonitrile → 4-Cyano-1-(2,6-difluorobenzyl)-1H-1,2,3-triazole
https://huagongshe.com/reaction/651242
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroacrylonitrile | HCID 70198 | — |
| Reactant | 2-(Azidomethyl)-1,3-difluorobenzene | HCID 10888323 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 4-Cyano-1-(2,6-difluorobenzyl)-1H-1,2,3-triazole | HCID 11042239 | — |
Reaction Steps
A mixture of 2,6-difluorobenzyl azide (34.2 g), 2-chloroacrylonitrile (26.6 g) and n-heptane (125 ml) is stirred at about 80° C. for 24 hours, whereby a suspension results. Unreacted 2-chloroacrylonitrile and 2,6-difluorobenzyl azide as well as n-heptane are distilled off (distillate 25 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 about 2 hours. The product is isolated by filtration, washed with n-heptane (100 ml) and dried in vacuo at about 60° C. Yield: 20.45 g=46.4% (beige powder).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06277999B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-c324893aeddc44eda9f5659721df773b |
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| Source note | uspto-grants-2001_08 |
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