Reacción #1269879

ord-8f603f8054224339b818b46fff4ae2bb

Ecuación de reacción

Oc1ccccc1
Phenol
O=C([O-])[O-].[K+].[K+]
K2CO3
C(=NC1CCCCC1)=NC1CCCCC1
DCC
O=C(O)c1cnccc1Cl
4-chloronicotinic acid
CCO
ethanol
CCOC(=O)c1cnccc1Oc1ccccc1
ethyl 4-phenoxynicotinate
Rendimiento 51.5%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe solid formed
  2. 2
    Filtraciónwas filtered off
  3. 3
    ExtracciónThe filtrate was extracted with DCM
  4. 4
    Lavadowashed with water
  5. 5
    Secadodried (MgSO4)
  6. 6
    Otrothe solvent was removed in vacuo
  7. 7
    workup.DISSOLUTIONThe crude ethyl 4-chloronicotinate (5.8 g) was dissolved in DMF (15 mL)
  8. 8
    TemperaturaThe reaction mixture was heated to 80° C. for 3 h
  9. 9
    Temperaturato cool to room temperature
  10. 10
    workup.WAITleft overnight
  11. 11
    workup.STIRRINGwithout stirring
  12. 12
    Extracciónextracted with EtOAc
  13. 13
    LavadoThe combined organic layers were washed with aqueous NaOH solution (1 M), water
  14. 14
    Secadodried over MgSO4
  15. 15
    OtroPurification by flash chromatography (DCM/EtOAc, gradient 1-10% EtOAc)

Procedimiento

DCC (5.24 g, 25.4 mmol) was added in portions over 10 min to a solution of 4-chloronicotinic acid (2.00 g, 12.7 mmol), ethanol (1.75 g, 38.1 mmol) and DMAP (0.19 g, 1.52 mmol) in DMF (20 mL) at 0° C. After stiffing for 1 h the reaction mixture was allowed to warm to room temperature and stirred overnight. Water (100 mL) was added and the solid formed was filtered off. The filtrate was extracted with DCM, washed with water, dried (MgSO4) and the solvent was removed in vacuo. The crude ethyl 4-chloronicotinate (5.8 g) was dissolved in DMF (15 mL). Phenol (2.86 g, 30.4 mmol), copper powder (0.48 g, 7.59 mmol), copper iodide (0.72 g, 3.80 mmol) and K2CO3 (4.20 g, 30.4 mmol) were added. The reaction mixture was heated to 80° C. for 3 h then allowed to cool to room temperature and left overnight without stirring. The mixture was poured into water and extracted with EtOAc. The combined organic layers were washed with aqueous NaOH solution (1 M), water and dried over MgSO4. Purification by flash chromatography (DCM/EtOAc, gradient 1-10% EtOAc) provided ethyl 4-phenoxynicotinate (1.59 g, 51% over 2 steps). ESI-MS [M+H]+=244.1.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08664214B2uspto-grants-2014_03