Reaktion #6266

ord-d824881d53434cb8beb91cc10043c497

Reaktionsgleichung

O=C1CSC(=S)N1
rhodanine
O=Cc1ccccc1
benzaldehyde
C1CCNCC1
piperidine
O=C1NC(=S)SC1=Cc1ccccc1
desired compound
Ausbeute 66.6%
O=C1NC(=S)SC1=Cc1ccccc1
5-benzylidenerhodanine
Ausbeute 66.6%

Reagenzien

Keine

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 10 g (75.1 mmol) of rhodanine and 7.63 ml (75.1 mmol) of benzaldehyde in 150 ml of ethanol, 0.74 ml (7.5 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 11.07 g of the desired compound (66.6% yield, pale yellow crystals).

Quelle

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