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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 587020Erstellt: 25. Oktober 2026

Ethyl bromopyruvate → Ethyl 2-methyl-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/587020

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromopyruvateHCID 66144—
EduktSodium BicarbonateHCID 516892—
EduktThioacetamideHCID 2723949—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 2-methyl-1,3-thiazole-4-carboxylateHCID 29335347,9%

Reaktionsschritte

To a solution of thioacetamide (11.9 g) in tetrahydrofuran (600 ml) was added sodium hydrogen carbonate (66.4 g), followed by addition of 80% ethyl bromopyruvate (50.0 g) at 0° C. The mixture was stirred overnight, the insolubles were filtered using Celite and the solvent was evaporated under reduced pressure. The resulting residue was dissolved in tetrahydrofuran (170 ml), and to the solution was added dropwise trifluoroacetic anhydride (170 ml) at 0° C., and the mixture was stirred at room temperature for 1 hour. To the mixture was added dropwise pyridine (200 ml) at 0° C., and the mixture was stirred at room temperature for 3 hours. The solvent was evaporated under reduced pressure, to the mixture was added ethyl acetate, and the mixture was washed with saturated sodium hydrogen carbonate solution and further with saturated brine and dried with magnesium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was purified with silica gel column chromatography (hexane:ethyl acetate=2:1) to give ethyl 2-methylthiazole-4-carboxylate (13.0 g) as brown crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06936602B1
Quelldatensatzuspto-grants-2005_08
ORD IDord-2df540d858d04c5ab7e61e69aa7b6f52
Quellennotizuspto-grants-2005_08