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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 386062Erstellt: 26. Oktober 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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic acid, azido-, ethyl esterHCID 69480—
Edukt2-Bromo-6-ethynylpyridineHCID 12970532—
EduktSodium AscorbateHCID 23667548—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
LösungsmittelSodium BicarbonateHCID 516892—
Produktethyl[4-(6-bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]acetateHCID 59525977—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367706B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-c07ac8fa129843fba3c3213505dc47fb
Quellennotizuspto-grants-2013_02