Aniline → N-Phenyl-2-furancarboxamide

HRID 582440

Reaktionsgleichung

Reaktionsgleichung von HRID 582440
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[O:15]1[CH:19]=[CH:18][CH:17]=[C:16]1[C:20](Cl)=[O:21]>ClCCl>[C:2]1([NH:1][C:20]([C:16]2[O:15][CH:19]=[CH:18][CH:17]=2)=[O:21])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
-10 °C

Versuchsvorschrift

N-phenyl furamide was prepared by adding to a mixture of aniline (23.3 g; 250 mmol) and triethylamine (25.3 g; 250 mmol) in dichloromethane slowly 32.6 g (250 mmol) of 2-furoyl chloride, while maintaining the temperature at -10° C. The product obtained was washed with diluted hydrochloric acid and water, dried with magnesium sulphate and evaporated. The product so obtained was than triturated with hexane and filtered. 39.3 g (84% yield of product was recovered.

Aufarbeitung

  1. customThe product obtained
  2. washwas washed with diluted hydrochloric acid and water
  3. dry with materialdried with magnesium sulphate
  4. customevaporated
  5. customThe product so obtained
  6. customthan triturated with hexane
  7. filtrationfiltered

Quellen und Nachweise

ORD-Eintrag
ord-ec294cbabf8b4576be6a8b4d93a811ec
Quelldatensatz
uspto-grants-1999_07
Patentnummer
US05925152

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