Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385940Generated: October 25, 2026

tert-Butanol → Ethyl[4-(6-chloropyridin-3-yl)-1H-1,2,3-triazol-1-yl]acetate

https://huagongshe.com/reaction/385940

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
Reactant2-Chloro-5-ethynylpyridineHCID 10654281—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
ProductEthyl[4-(6-chloropyridin-3-yl)-1H-1,2,3-triazol-1-yl]acetateHCID 59526155—

Reaction Steps

2-Chloro-5-ethynylpyridine (100 mg, 0.73 mmol) and ethylazidoacetate (0.41 ml, 0.73 mmol) were taken up in water (1.5 ml) and 2-methylpropan-2-ol (1.5 ml) at room temperature. Aqueous solutions of copper(II) sulfate pentahydrate (9.08 mg, 0.036 mmol) in 1 mL of water and L-sodium ascorbate (28.8 mg, 0.145 mmol) in 1 mL of water were sequentially added, and the reaction was stirred at room temperature for 18 hours. The reaction was then quenched with saturated aqueous sodium bicarbonate, and extracted three times with ethyl acetate. The organic layers were combined, dried over anhydrous magnesium sulfate, filtered, and concentrated. The resulting crude product was purified by silica gel chromatography (0-65% ethyl acetate/hexanes) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-e75d9aa5fa72495d94759eff5ef55cbc
Source noteuspto-grants-2013_02