Reaktion #360849

ord-754941a70720496981da1d5a812e9111

Reaktionsgleichung

O
water
O=C(O)CC(=O)O
Malonic acid
O=Cc1ccco1
furfural
O=C(O)C=Cc1ccco1
2-furanacrylic acid
Ausbeute 18.1%

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigepumped through the CMR (15 ml/min; 165° C.; 1200 kPa)
  2. 2
    Waschenwashed with 5% aqueous sulphuric acid (4×200 ml)
  3. 3
    Sonstigeto remove most of the pyridine
  4. 4
    SonstigeThe remaining solution was evaporated to dryness on a rotary evaporator

Vorschrift

Malonic acid (104 g; 1 mole) was dissolved in a mixture of furfural (96 g; 1 mole), pyridine (72 ml) and ethanol (10 ml) and pumped through the CMR (15 ml/min; 165° C.; 1200 kPa). The product mixture was diluted with diethyl ether (200 ml) and washed with 5% aqueous sulphuric acid (4×200 ml) to remove most of the pyridine. The remaining solution was evaporated to dryness on a rotary evaporator and the resultant 2-furanacrylic acid (25 g; 18% yield) crystallised from water m. p. 141° C. The MS was in close agreement with spectrum in the MS library. For a convention preparation see ref.18.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05387397uspto-grants-1995_02