Reacción #1269879
ord-8f603f8054224339b818b46fff4ae2bb
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Otrothe solid formed
- 2Filtraciónwas filtered off
- 3ExtracciónThe filtrate was extracted with DCM
- 4Lavadowashed with water
- 5Secadodried (MgSO4)
- 6Otrothe solvent was removed in vacuo
- 7workup.DISSOLUTIONThe crude ethyl 4-chloronicotinate (5.8 g) was dissolved in DMF (15 mL)
- 8TemperaturaThe reaction mixture was heated to 80° C. for 3 h
- 9Temperaturato cool to room temperature
- 10workup.WAITleft overnight
- 11workup.STIRRINGwithout stirring
- 12Extracciónextracted with EtOAc
- 13LavadoThe combined organic layers were washed with aqueous NaOH solution (1 M), water
- 14Secadodried over MgSO4
- 15OtroPurification 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.