Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
ReactantSodium AzideHCID 33557—
SolventEthanolHCID 702—
Product4-(Azidomethyl)-1,2-dichlorobenzeneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950673
Source datasetuspto-grants-1990_08
ORD IDord-897a2ce76b224df291c6193ab7a46eea
Source noteuspto-grants-1990_08