Reacción #6913
ord-50a401181684469192a5170e3a2ba065
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroPrepared
- 2Temperaturawarmed
- 3Temperaturato reflux under N2
- 4Temperaturaat reflux
- 5TemperaturaAfter cooling
- 6Otrothe reaction to rt
- 7OtroThe volatiles were removed
- 8workup.ADDITIONfrexh methanol was added to the resulting residue
- 9OtroAgain, the volatiles were removed
- 10Lavadowashed with saturated potassium carbonate (aqueous)
- 11SecadoThe organic layer was dried over sodium sulfate
- 12Otrothe volatiles were removed
Procedimiento
Prepared according to Procedure K. 2-iso-Propylsulfonylacetonitrile (0.50 g, 3.39 mmol) was dissolved in THF and warmed to reflux under N2. Borane dimethylsulfide (2M, 1.7 mL, 3.39 mmol) was added dropwise and the reaction was stirred for an additional 40 minutes at reflux. After cooling the reaction to rt, HCl (2 M in MeOH) was added to the reaction slowly due to gas evolution. The volatiles were removed and frexh methanol was added to the resulting residue. Again, the volatiles were removed and the resulting residue was taken up in CH2Cl2 (25 mL) and washed with saturated potassium carbonate (aqueous). The organic layer was dried over sodium sulfate and the volatiles were removed to afford the title compound. GC-MS m/z 152 (MH+).