Reacción #582503

ord-affe587f4e1d4c599e66c79b12e2f716

Ecuación de reacción

O=C1CCCCC1
Cyclohexanone
[Na+].[OH-]
sodium hydroxide
CCCCCCOc1ccc(C=O)cc1
4-Hexyloxybenzaldehyde
CCCCCCOc1ccc(C=C2CCCC(=Cc3ccc(OCCCCCC)cc3)C2=O)cc1
2,6-Bis-(4-hexyloxy-benzylidene)-cyclohexanone

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for 16 h
  3. 3
    OtroA yellow crystalline solid was isolated by vacuum filtration
  4. 4
    Lavadowas washed with cold ethanol
  5. 5
    Otrodried in a vacuum oven

Procedimiento

Cyclohexanone (2.6 ml, 0.025 mol) was dissolved in ethanol (5 ml), and was added to sodium hydroxide (0.38 g, 0.01 mol) dissolved in water (6 ml) and ethanol (2 ml) and was left to stir for 20 min. 4-Hexyloxybenzaldehyde (10 ml, 0.048 mol), dissolved in ethanol (40 ml), was added and the mixture was stirred at room temperature for 16 h. A yellow crystalline solid was isolated by vacuum filtration and was washed with cold ethanol and dried in a vacuum oven. Yield=4.32 g, 36%. 1H NMR and 13C NMR showed expected signals.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06939479B2uspto-grants-2005_09