Reacción #84400
ord-ae6ec9c3bee54ec0aec43474a3191766
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Concentraciónconcentrated in vacuo
- 2workup.DISSOLUTIONThe residue was dissolved in water (100 mL)
- 3Extracciónextracted with CH2Cl2 (100 mL×3)
- 4LavadoThe combined organic phases were washed with brine (150 mL)
- 5Secadodried over anhydrous Na2SO4
- 6Concentraciónconcentrated in vacuo
Procedimiento
A solution of tert-butyl (3-morpholinophenyl)carbamate (5.91 g, 21.20 mmol) in a solution of HCl (106 mL, 106.0 mmol, 1 M in MeOH) was stirred at rt overnight, then concentrated in vacuo. The residue was dissolved in water (100 mL). The soltution was basified with saturated Na2CO3 aqueous solution and extracted with CH2Cl2 (100 mL×3). The combined organic phases were washed with brine (150 mL), dried over anhydrous Na2SO4 and concentrated in vacuo to give the title compound as a light brown solid (3.42 g, 91%).