Reaktion #159955

ord-fb2dddac9b4b492ab2f73cd7baa61606

Reaktionsgleichung

CCOC(=O)c1[nH]c(C=O)cc1C
Ethyl 5-formyl-3-methyl-1H-pyrrole-2-carboxyate
CCOC(=O)CC(=O)[O-]
monoethyl malonate
C1CCNCC1
piperidine
CCOC(=O)/C=C/c1cc(C)c(C(=O)OCC)[nH]1
title compound
Ausbeute 47.7%
CCOC(=O)/C=C/c1cc(C)c(C(=O)OCC)[nH]1
Ethyl 5-[(E)-2-ethoxycarbonylvinyl]-3-methyl-1H-pyrrole-2-carboxyate
Ausbeute 47.7%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationthe precipitate was recovered by filtration
  2. 2
    WaschenThe precipitate was washed with water
  3. 3
    Sonstigedried
  4. 4
    Temperaturunder heating

Vorschrift

Ethyl 5-formyl-3-methyl-1H-pyrrole-2-carboxyate 470 mg, monoethyl malonate 378 mg, piperidine 0.05 mL and pyridine 6 mL were mixed and stirred at 100° C. for 38 hours. Ice water was added to the reaction liquid and the precipitate was recovered by filtration. The precipitate was washed with water and dried in flowing air under heating to provide 311 mg of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08829000B2uspto-grants-2014_09