Reaction #2275694

ord-8f8d2241ef70466d9a57ed3a7f9ce70a

Reaction equation

N#Cc1ncc(Cl)cc1Cl
3,5-dichloro-2-cyanopyridine
OCc1ccccc1
benzyl alcohol
[H-].[Na+]
sodium hydride
[H][H]
hydrogen
N#Cc1ncc(OCc2ccccc2)cc1OCc1ccccc1
desired compound
Yield 94.0%
N#Cc1ncc(OCc2ccccc2)cc1OCc1ccccc1
3,5-bis-benzyloxy-pyridine-2-carbonitrile
Yield 94.0%

Solvents

Conditions

Temperature
0°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperatureto warm to room temperature
  2. 2
    TemperatureThe solution is re-cooled to 0° C.
  3. 3
    Otheris transferred to an unfocussed Mars 5 CEM microwave reactor to 190° C.
  4. 4
    OtherThe reaction mixture is quenched with H2O
  5. 5
    Concentrationconcentrated under reduced pressure
  6. 6
    workup.ADDITIONdiluted with EtOAc
  7. 7
    Washwashed with 2M Na2CO3, H2O and saturated aqueous NaCl
  8. 8
    DryingThe organic layer is dried (MgSO4)
  9. 9
    Filtrationfiltered
  10. 10
    Concentrationconcentrated under reduced pressure
  11. 11
    Otherto give a brown solid
  12. 12
    OtherThe crude solid is purified over silica (EtOAc:heptane, gradient 1:1 to 1:0)

Procedure

To an 80 mL microwave pressure vessel is charged dry THF (30 mL) and benzyl alcohol (6.32 mL, 61.1 mmol). The solution is cooled to 0° C. and sodium hydride (2.44 g of a 60% dispersion in mineral oil, 61.1 mmol) is added in portions. The reaction mixture is gradually allowed to warm to room temperature with efficient stirring until the evolution of hydrogen gas ceases. The solution is re-cooled to 0° C. and 3,5-dichloro-2-cyanopyridine (5.00 g, 29.1 mmol) is added, and the solution is transferred to an unfocussed Mars 5 CEM microwave reactor to 190° C., 300 W and held for 5 hours. The reaction mixture is quenched with H2O, concentrated under reduced pressure, diluted with EtOAc and washed with 2M Na2CO3, H2O and saturated aqueous NaCl. The organic layer is dried (MgSO4), filtered and concentrated under reduced pressure to give a brown solid. The crude solid is purified over silica (EtOAc:heptane, gradient 1:1 to 1:0) to afford 8.6 g (94% yield) of the desired compound as an orange solid. 1H NMR (400 MHz, CDCl3) δ ppm 7.96 (1H, d, J=2.2 Hz), 7.25-7.37 (10H, m), 6.78 (1H, d, J=2.2 Hz), 5.10 (2H, s), 5.03 (2H, s). HPLC-MS: m/z 317 [M+H]+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08323671B2uspto-grants-2012_12