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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1914593Erstellt: 25. Oktober 2026

Formamide → 5-Oxazol-4-yl-thiophene-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/1914593

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormamideHCID 713—
EduktSulfuric AcidHCID 1118—
Edukt5-(2-Bromo-acetyl)-thiophene-3-carboxylic acid methyl esterHCID 53904546—
Produkt5-Oxazol-4-yl-thiophene-3-carboxylic acid methyl esterHCID 58110244—

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

5-(2-Bromo-acetyl)-thiophene-3-carboxylic acid methyl ester (0.60 g, 2.28 mmol) was suspended in formamide (10 mL) then sulfuric acid (1 mL) was added and the tube purged with nitrogen then sealed. The mixture was heated at 150° C. by microwave irradiation for 15 minutes. The resultant solution was diluted with HCl (1 N) and water and extracted with ethyl acetate (×3). The organic phase was dried over sodium sulfate and evaporated then purified by chromatography on a silica II cartridge, eluting with 1:1 DCM:cyclohexane to afford 5-oxazol-4-yl-thiophene-3-carboxylic acid methyl ester as a pale yellow solid (0.197 g). LCMS m/z 210.14 [M+H]+ R. T.=3.64 min (Analytical Method 9).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08614209B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-81f9109593554d81b4f5f8e543e1fb83
Quellennotizuspto-grants-2013_12