Reaktion #82110

ord-497d9d70153746f4a8ae84d7bcf9cb93

Reaktionsgleichung

O=S(=O)(O)O
sulfuric acid
CCOc1cc(C=O)ccc1O
3-ethoxy-4-hydroxybenzaldehyde
Nc1ccccc1
aniline
O=C(O)CC(=O)O
Malonic acid
CCOc1cc(C=CC(=O)O)ccc1O
compound
Ausbeute 56.1%
CCOc1cc(C=CC(=O)O)ccc1O
3-ethoxy-4-hydroxycinnamic acid
Ausbeute 56.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe crude crystals were obtained by filtration
  2. 2
    Waschenwashed with water
  3. 3
    Sonstigedried

Vorschrift

Malonic acid (1.56 g) and pyridine (3.0 ml) were placed in an egg-plant type flask (100 ml). Further, 3-ethoxy-4-hydroxybenzaldehyde (1.66 g) and aniline (30 μl) were added thereto and a reaction was performed at 55° C. for 3 hours. The reaction solution was acidified by adding dilute sulfuric acid. The crude crystals were obtained by filtration, washed with water, and then dried to obtain the above-identified compound (1.1 g, 56.1%) as a light yellowish crystal. Melting point: 157°-158° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05621009uspto-grants-1997_04