Реакция #54278

ord-68adba173cd44fdbb7ecad9cbd0a1ec0

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураAfter cooling
  2. 2
    Другоеthe ethanol and excess amine are removed by distillation under reduced pressure
  3. 3
    ЭкстракцияThe residue is extracted with 100 ml
  4. 4
    Промывкаof 1N HCl and the extract is washed twice with 50 ml
  5. 5
    ЭкстракцияThe hydrochloric acid extract
  6. 6
    Экстракцияthe liberated oil is extracted with ether
  7. 7
    ЭкстракцияThe ether extract
  8. 8
    Другоеis dried
  9. 9
    workup.ADDITIONan etherial hydrochloric acid solution is added
  10. 10
    Фильтрацияis filtered
  11. 11
    Другоеdried
  12. 12
    ДругоеUpon recrystallization of the crude crystals from isopropyl alcohol, 6.4 g

Методика

20.5 g. of 1-(3,4-methylenedioxyphenyl)-2-chloroethanol are mixed with 30 g. of isopropylamine and 100 ml. of ethanol and the mixture is refluxed for 8 hours. After cooling, the ethanol and excess amine are removed by distillation under reduced pressure. The residue is extracted with 100 ml. of 1N HCl and the extract is washed twice with 50 ml. of ether. The hydrochloric acid extract is made basic with 1N caustic soda, and the liberated oil is extracted with ether. The ether extract is dried and an etherial hydrochloric acid solution is added. The crystalline hydrochloride settles out of solution and is filtered and dried. Upon recrystallization of the crude crystals from isopropyl alcohol, 6.4 g. of 1 -(3,4-methylenedioxyphenyl)-2-isopropylaminoethanol hydrochloride are obtained.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04147799uspto-grants-1979_04