Réaction #833511

ord-a85e475e5a284b7cb732c9fb8d9f8aa3

Équation de réaction

C=CCOc1ccc(C=O)cc1OC
3-Methoxy-4-(2-propenyloxy)benzaldehyde
[Na+].[OH-]
sodium hydroxide
Cc1cc(C)cc(C)c1
mesitylene
C=CCc1cc(C=O)cc(OC)c1O
3-allyl-4-hydroxy-5-methoxybenzaldehyde

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureAfter cooling
  2. 2
    LavageThe aqueous phase was washed two times with diethyl ether
  3. 3
    Extractionextracted with ethyl acetate
  4. 4
    AutreAfter drying
  5. 5
    Concentrationconcentrating the organic phase, there
  6. 6
    Autrethat crystallized
  7. 7
    Températureon cooling

Mode opératoire

3-Methoxy-4-(2-propenyloxy)benzaldehyde (19.7 g, 0.100 mol) was heated under reflux in 75 ml mesitylene (1,3,5-trimethylbenzene) for 20 hours. After cooling, 250 ml 2N sodium hydroxide were added to the reaction mixture. The aqueous phase was washed two times with diethyl ether. The aqueous phase was subsequently acidified with concentrated hydrochloric acid under ice cooling and then extracted with ethyl acetate. After drying and concentrating the organic phase, there remained a light orange-colored oil that crystallized on cooling.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07393367B2uspto-grants-2008_07