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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 357768Erstellt: 24. Oktober 2026

Dimethylformamide → 2,5-Dimethylthiophene-3-carbaldehyde

https://huagongshe.com/de/reaction/357768

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt2,5-DimethylthiopheneHCID 12514—
EduktPhosphorus oxychlorideHCID 24813—
LösungsmittelWaterHCID 962—
Produkt2,5-Dimethylthiophene-3-carbaldehydeHCID 276275910,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Phosphorus oxychloride (10 ml) was slowly added dropwise to dimethylformamide (30 g) under ice-cooling, and 2,5-dimethylthiophene (11.2 g) was added. The mixture was stirred at 100° C. for 15 hours, poured into water and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 2,5-dimethyl-3-thiophenecarbaldehyde (1.41 g). 2,5-Dimethyl-3-thiophenecarbaldehyde (3.89 g) synthesized in this manner was dissolved in acetonitrile (30 ml), and sodium dihydrogen phosphate (1.2 g) in water (15 ml) and 30% aqueous hydrogen peroxide (3.5 ml) were added dropwise. The mixture was stirred at room temperature for 2 hours, alkalified with 1N aqueous sodium hydroxide and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 2,5-dimethyl-3-thiophenecarboxylic acid (4.09 g) as crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05840917
Quelldatensatzuspto-grants-1998_11
ORD IDord-5f2562df807c47ee9af68f2b2cff287a
Quellennotizuspto-grants-1998_11