Reaktion #6270

ord-06a787a9c29b4bc098767573585c59cc

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 12.5 g (107 mmol) of 2,4-thiazolidinedione and 25.0 g (107 mmol) of 3,5-di-tert-butyl-4-hydroxybenzaldehyde in 300 ml of ethanol, 1.05 ml (10.7 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 15.23 g of the desired compound (42.8% yield, pale yellow crystals).

Quelle

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