Reacción #1461440
ord-6ef711e8dd37421a9ddfde4b2321820e
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroPreparation H1, Step 2
- 2Otroto come to room temperature
- 3Otroreaction
- 4workup.STIRRINGthe reaction was stirred for an additional 2 h
- 5Otrothe residue was partitioned between ethyl acetate and saturated sodium bicarbonate
- 6OtroThe layers were separated
- 7Lavadothe organic phase was washed 2× with saturated sodium bicarbonate
- 8Extracciónthe combined aqueous phases were extracted with ethyl acetate
- 9Lavadothe combined organic phases were washed with brine
- 10Secadodried over sodium sulfate
- 11Concentraciónconcentrated in vacuo
- 12OtroThe residue was purified over silica gel
- 13Lavadoeluting with 20% ethyl acetate/heptane
Procedimiento
Preparation H1, Step 2: A solution of 2-phenylisonicotinic acid (459 mg, 2.30 mmol) in 9:1 benzene/methanol (20 mL) was cooled to 0° C., and treated with the dropwise addition of a 2.0 M hexane solution of (trimethylsilyl)diazomethane (1.15 mL, 2.30 mmol). The mixture was allowed to come to room temperature and stirred for 6 h. Analysis by TLC indicated incomplete reaction, so the mixture was treated with additional (trimethylsilyl)diazomethane solution (230 μL, 0.23 mmol), and the reaction was stirred for an additional 2 h. TLC of the mixture remained unchanged. The solvent was stripped, and the residue was partitioned between ethyl acetate and saturated sodium bicarbonate. The layers were separated, the organic phase was washed 2× with saturated sodium bicarbonate, the combined aqueous phases were extracted with ethyl acetate, and the combined organic phases were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified over silica gel, eluting with 20% ethyl acetate/heptane, to yield 372 mg of methyl 2-phenylisonicotinate as a colorless oil. 1H NMR (400 MHz, CDCl3) δ ppm 8.83 (d, J=5.27 Hz, 1H), 8.29 (s, 1H), 8.04 (d, J=7.03 Hz, 2H), 7.77 (d, J=3.52 Hz, 1H), 7.51–7.42 (m, 3H), 3.98 (s, 3H).