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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753813Generated: October 28, 2026

Hydrochloric Acid → ethyl 2-(4-cyano-1H-1,2,3-triazol-1-yl)acetate

https://huagongshe.com/reaction/1753813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
Reactant2-ChloroacrylonitrileHCID 70198—
SolventWaterHCID 962—
Productethyl 2-(4-cyano-1H-1,2,3-triazol-1-yl)acetateHCID 54053451—

Reaction Steps

4.1 g (31.9 mmol) azidoacetic acid ethyl ester and 2.8 g (31.9 mmol) 2-chloroacrylonitrile are stirred in 32 ml water at a bath temperature of 80° C. for 16 h. After cooling to RT, the solution is rendered acid with 1 N hydrochloric acid and extracted with ethyl acetate. The organic phase is dried over sodium sulfate, filtered and concentrated in vacuo. 50 ml ethanol and 10 drops of conc. sulfuric acid are added to the residue and the mixture is stirred under reflux for 16 h. For working up, the reaction mixture is concentrated in vacuo, ethyl acetate is added to the residue, the suspension is washed with half-concentrated sodium bicarbonate solution and the organic phase is dried over sodium sulfate. The solvent is removed completely on a rotary evaporator and the solid is dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09168249B2
Source datasetuspto-grants-2015_10
ORD IDord-460689f3fd1e4cf7b760c143aa4f4314
Source noteuspto-grants-2015_10