Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386062Generated: October 26, 2026

Acetic acid, azido-, ethyl ester → ethyl[4-(6-bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]acetate

https://huagongshe.com/reaction/386062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
Reactant2-Bromo-6-ethynylpyridineHCID 12970532—
ReactantSodium AscorbateHCID 23667548—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventSodium BicarbonateHCID 516892—
Productethyl[4-(6-bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]acetateHCID 59525977—

Reaction Steps

2-Bromo-6-ethynylpyridine (Example 465, Step 1) (350 mg, 1.92 mmol) and ethyl azidoacetate (1.08 ml, 1.92 mmol) were combined in t-BuOH (4.0 mL) and water (2.0 mL). CuSO4.5H2O (24 mg, 0.096 mmol) in water (1.0 mL) was added, followed by sodium ascorbate (76 mg, 0.39 mmol) in water (1.0 mL). The reaction was stirred at room temperature for 5 h, diluted with saturated NaHCO3, and extracted with EtOAc (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered, and evaporated to a yellow residue that was purified by flash chromatography (0-30% EtOAc/hexanes) to afford the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-c07ac8fa129843fba3c3213505dc47fb
Source noteuspto-grants-2013_02