Реакция #4300

ord-5b62d5e0639c4fe99fa536f8aadfd356

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solvent was removed in vacuo
  2. 2
    Другоеthe residue was partitioned between methylene chloride and dilute sodium hydroxide
  3. 3
    СушкаThe methylene chloride solution was dried over magnesium sulfate
  4. 4
    Другоеthe solvent was removed in vacuo
  5. 5
    Другоеto give an oil
  6. 6
    workup.ADDITIONwas added
  7. 7
    ДругоеA 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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04724235uspto-grants-1988_02