HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709658Generated: October 30, 2026
3,4-Dichlorobenzyl chloride → 4-(Azidomethyl)-1,2-dichlorobenzene
https://huagongshe.com/reaction/1709658
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-Dichlorobenzyl chloride | HCID 7609 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Azidomethyl)-1,2-dichlorobenzene | HCID 15065218 | — |
Reaction Steps
A stirred mixture of 3,4-dichlorobenzyl chloride (12.6 g, 64.5 mmol) and sodium azide (7.0 g, 0.11 mole) in absolute ethanol (70 ml) was refluxed for 4.75 hours, cooled and filtered to provide a solution of 3,4-dichlorobenzyl azide. Separately, 2-cyanoacetamide (5.5 g, 65 mmol) was added to a 35° C. solution of sodium (1.5 g, 65 mmol) in absolute ethanol (125 ml), and to the resulting suspension was added the above azide solution dropwise over 10 minutes. The combined mixtures were refluxed for 1 hour, kept 16 hours at ambient temperature and 1 hour at 5° C., and filtered. The crude product was dried under vacuum, dissolved in boiling ethanol (290 ml), filtered hot, and cooled to 0° C. The solid was collected by filtration and dried under vacuum to provide 12.4 g (67%) of 1-(3,4-dichlorobenzyl)-5-amino-1,2,3-triazole-4-carboxamide, m.p 221°-222° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04950673 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-897a2ce76b224df291c6193ab7a46eea |
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| Source note | uspto-grants-1990_08 |
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