Reacción #1885000

ord-b743269aac2642f9b3b687f5699031a3

Ecuación de reacción

O=C(O)C=Cc1ccc(F)c(F)c1
3,4-di-fluoro-cinnamic acid
OCC1CC2C=CC1C2
5-norbornene-2-methanol
Cc1ccccc1C
xylene
C1=CC2CCC1C2.Cc1c(C=CC(=O)[O-])ccc(F)c1F
5-norbornene 2-methyl-(3,4-di-fluoro-cinnamate)
Rendimiento 63.0%

Disolventes

Condiciones de reacción

Temperatura
145°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaazeotropically refluxed for 24 hours
  2. 2
    OtroAfter the reaction
  3. 3
    Temperaturathe mixture cooled down to room temperature
  4. 4
    ExtracciónThe resulting product was extracted by 1M HCl
  5. 5
    Lavadowashed again with water
  6. 6
    SecadoThe organic layer was dried with Na2SO4
  7. 7
    Otrothe solvent was evaporated out
  8. 8
    Otroto give a highly viscous material

Procedimiento

5 g (27.2 mmol) of 3,4-di-fluoro-cinnamic acid, 3.38 g (1 eq.) of 5-norbornene-2-methanol, and 0.13 g (0.02 eq.) of zirconium(IV) acetate hydroxide were added to 50 ml of xylene and stirred. The mixture was heated to 145° C. under N2 atmosphere and azeotropically refluxed for 24 hours. After the reaction, the mixture cooled down to room temperature and was added with 100 volume % of ethyl acetate. The resulting product was extracted by 1M HCl and washed again with water. The organic layer was dried with Na2SO4 and the solvent was evaporated out to give a highly viscous material. (Yield: 63%, Purity (GC): 80%)

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08343597B2uspto-grants-2013_01