Reaktion #6264

ord-f99fd64ecadc4d6fbfc0db3ce5607ef8

Reaktionsgleichung

O=C1CSC(=O)N1
2,4-thiazolidinedione
O=Cc1ccccc1
benzaldehyde
C1CCNCC1
piperidine
O=C1NC(=O)C(=Cc2ccccc2)S1
desired compound
Ausbeute 90.4%
O=C1NC(=O)C(=Cc2ccccc2)S1
5-benzylidene-2,4-thiazolidinedione
Ausbeute 90.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was heated
  2. 2
    Temperaturunder reflux for 5 hours
  3. 3
    TemperaturAfter cooling
  4. 4
    Filtrationthe precipitated crystals were filtered
  5. 5
    Waschenwashed with cooled ethanol

Vorschrift

To a solution of 20 g (171 mmol) of 2,4-thiazolidinedione and 17.4 ml (171 mmol) of benzaldehyde in 350 ml of ethanol, 1.68 ml (17.1 mmol) of piperidine was added, and the mixture was heated under reflux for 5 hours. After cooling, the precipitated crystals were filtered and washed with cooled ethanol to give 31.67 g of the desired compound (90.4% yield, pale yellow crystals).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05246948uspto-grants-1993_09