Reacción #4297
ord-ae4c77ae86b04fcaa9012d4cce7a5a3a
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroThe solvent is removed in vacuo
- 2Otrothe residue is partitioned between methylene chloride and dilute sodium hydroxide
- 3ExtracciónThe methylene chloride solution is extracted with dilute sulfuric acid
- 4ExtracciónThe acidic extract
- 5Extracciónthe basic solution is extracted with methylene chloride
- 6SecadoThe methylene chloride solution is dried over magnesium sulfate
- 7Otrothe solvent is removed in vacuo
Procedimiento
A solution of 2-chloroethylphenyl sulfone and a large excess of methylamine (40% solution in water) in acetonitrile is stirred at room temperature overnight. The solvent is removed in vacuo and the residue is partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution is extracted with dilute sulfuric acid. The acidic extract is made basic with 50% sodium hydroxide and the basic solution is extracted with methylene chloride. The methylene chloride solution is dried over magnesium sulfate and the solvent is removed in vacuo to give the title compound.