HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353380Generated: October 31, 2026
2-Chloroacrylonitrile → 4-Cyano-1-(2,6-difluorobenzyl)-1H-1,2,3-triazole
https://huagongshe.com/reaction/2353380
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroacrylonitrile | HCID 70198 | — |
| Reactant | 2-(Azidomethyl)-1,3-difluorobenzene | HCID 10888323 | — |
| Solvent | Water | HCID 962 | — |
| 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 (17.73 g) and water (125 ml) is stirred for 24 hours at about 80°C. By increasing the external temperature to about 130°C., excess 2-chloroacrylonitrile is distilled off. The semisolid mixture is cooled to about 40°C., cyclohexane (50 ml) is added to the suspension and the mixture is brought to about 20°C.and stirred for about 2 hours. The product is isolated by filtration and washed with cyclohexane (75 ml) and then with water (50 ml). The moist product is mixed with water (100 ml), the suspension is filtered and the product is washed with water (50 ml) and dried at about 60°C. in vacuo. Yield: 38.04 g =86%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750028B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-94cf4427043e41f7a0bd38fe6309e94b |
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| Source note | uspto-grants-2010_07 |
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