Reaktion #62352

Reaktionsgleichung

acetic acid (2-chloro-5-cyanothiophen-3-ylmethylene)hydrazide

potassium acetate

→

title compound

Ausbeute 10.1%

1-Acetyl-1H-thieno[2,3-c]pyrazole-5-carbonitrile

Ausbeute 10.1%

Lösungsmittel

diphenyl ether

Reaktionsbedingungen

Aufarbeitung

1. 1
   Filtrationfiltration through Celite
2. 2
   Waschenthe filtrate was washed successively with saturated aqueous ammonium chloride and saturated brine
3. 3
   Trocknendried over anhydrous magnesium sulfate
4. 4
   Sonstigethe solvent was evaporated
5. 5
   SonstigeThe crude product was purified
6. 6
   Sonstigeseparated by silica gel column chromatography (ethyl acetate:n-hexane=1:10-1:5)

Vorschrift

To a solution of 2.53 g of acetic acid (2-chloro-5-cyanothiophen-3-ylmethylene)hydrazide in 22 mL of diphenyl ether were added copper powder and potassium acetate at room temperature, and stirred at 200° C. for 6 hours. Following filtration through Celite, the filtrate was washed successively with saturated aqueous ammonium chloride and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=1:10-1:5), to afford 215 mg of the title compound as colorless crystals.

Quelle