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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 928529Erstellt: 25. Oktober 2026

Acetic acid, azido-, ethyl ester → Ethyl 2-azido-3-(5-bromothiophen-2-yl)acrylate

https://huagongshe.com/reaction/928529

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic acid, azido-, ethyl esterHCID 69480—
Edukt5-Bromothiophene-2-carbaldehydeHCID 78428—
EduktSodiumHCID 5360545—
LösungsmittelEthanolHCID 702—
ProduktEthyl 2-azido-3-(5-bromothiophen-2-yl)acrylateHCID 7316697742%

Reaktionsschritte

A solution of sodium (2.76 g, 120 mmol) in absolute EtOH (120 mL) was cooled in an ice-bath and a mixture of 5-bromo-2-formylthiophene (5.73 g, 30 mmol) and ethyl azidoacetate (15.49 g, 120 mmol) was added dropwise during 30 min period. The bath was removed and the reaction mixture was stirred at room temperature for another 30 min. A cold solution of saturated aqueous NH4Cl solution (100 mL) was added and the resulting solution was extracted with diethyl ether (3×100 mL) and the combined organic layers were washed with brine (200 mL), dried over Na2SO4. After removing diethyl ether under reduced pressure, the crude product was purified by column chromatography (EtOAc/Hexane: 1/50) to give acrylate 60 (3.81 g, 42%) as a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09290512B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-a8aa6b9367c44f35b21ce49fead0f8ef
Quellennotizuspto-grants-2016_03