Reaktion #65255

ord-9f5c38a8d3ec4df8a69471349893b3ad

Reaktionsgleichung

CCCCc1ncc(C=O)n1Cc1ccccc1Cl
2-n-butyl-1-(2-chlorophenyl)methyl-1H-imidazol-5-carboxaldehyde
O=C(O)Cc1cccs1
2-thienylacetic acid
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(=O)OC(C)=O
acetic anhydride
CCCCc1ncc(/C=C(\C(=O)O)c2cccs2)n1Cc1ccccc1Cl
title compound
CCCCc1ncc(/C=C(\C(=O)O)c2cccs2)n1Cc1ccccc1Cl
(E)-3-[2-n-Butyl-1-{(2-chlorophenyl)methyl}-1H-imidazol-5-yl]-2-(2-thienyl)-2-propenoic Acid

Lösungsmittel

Reaktionsbedingungen

Temperatur
140°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe cooled reaction
  2. 2
    Sonstigethe solid is separated
  3. 3
    Sonstigetriturated several times with ether
  4. 4
    Sonstigethe solid is crystallized

Vorschrift

A mixture of 2-n-butyl-1-(2-chlorophenyl)methyl-1H-imidazol-5-carboxaldehyde (2 mmol), 2-thienylacetic acid (2.3 mmol), potassium carbonate (0.91 mmol), and acetic anhydride (1 mL) is heated gradually to 140° C. and held at this temperature for 6 hours. The cooled reaction is diluted with water and the solid is separated, triturated several times with ether, and the solid is crystallized to give the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05418250uspto-grants-1995_05