Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562444Generated: October 31, 2026

Ethyl bromoacetate → Ethyl 2-(1H-1,2,3-triazol-1-YL)acetate

https://huagongshe.com/reaction/562444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodiumHCID 5360545—
ReactantHCID 178418936HCID 178418936—
SolventEthanolHCID 702—
ProductEthyl 2-(1H-1,2,3-triazol-1-YL)acetateHCID 10103365—

Reaction Steps

129.2 g (5.6 mmol) of sodium are added slowly to 4.0 litres of ethanol. 400.0 g (5.6 mol) of 1,2,3-1H-triazole are then added, and 623 ml (938.2 g, 5.6 mol) of ethyl bromoacetate are added dropwise at an internal temperature of 20-25° C. The mixture is stirred at RT for 48 h. The precipitated solid is filtered off, the ethanol is removed under reduced pressure and the mixture is filtered again. The residue is taken up in ethyl acetate, filtered, again concentrated under reduced pressure and purified by distillation on a 30 cm column. The product is obtained at a bath temperature of 140° C., a head temperature of 60-115° C. and a pressure of 1 mbar. Yield: 440.0 g (50% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067407B2
Source datasetuspto-grants-2011_11
ORD IDord-951eeb148d06444b83c2c93ba618087f
Source noteuspto-grants-2011_11