Реакция #4300
ord-5b62d5e0639c4fe99fa536f8aadfd356
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ДругоеThe solvent was removed in vacuo
- 2Другоеthe residue was partitioned between methylene chloride and dilute sodium hydroxide
- 3СушкаThe methylene chloride solution was dried over magnesium sulfate
- 4Другоеthe solvent was removed in vacuo
- 5Другоеto give an oil
- 6workup.ADDITIONwas added
- 7ДругоеA white solid precipitated
Методика
A mixture of 70.23 g (0.344 mole) of 2-chloroethylphenylsulfone, 41.92 g (0.343 mole) of phenethylamine and 60 ml of triethylamine in 800 ml of acetonitrile was stirred at room temperature for 18 hr. The solvent was removed in vacuo, and the residue was partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution was dried over magnesium sulfate, and the solvent was removed in vacuo to give an oil. This was dissolved in methanol and excess of ethereal hydrogen chloride was added and ether was added. A white solid precipitated to give 68.39 g (60%) of white crystalline solid, m.p. 194°-196° C.