Реакция #55570

ord-e7c5f52d7e334538a14be7fc7523ef98

Условия реакции

Температура
130°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеto react at 120° C
  2. 2
    ТемператураThis reaction mixture was heated to about 150° C.
  3. 3
    ТемператураThe mixture was cooled
  4. 4
    Экстракцияextracted with 600 ml (3×300 ml) of ether
  5. 5
    Экстракцияextracted with 600 ml (2×300 ml) of ether
  6. 6
    ЭкстракцияThe combined ether extract
  7. 7
    Промывкаwas washed with 200 ml of saturated aqueous sodium chloride
  8. 8
    Сушкаdried over anhydrous magnesium sulfate
  9. 9
    Фильтрацияfiltered
  10. 10
    Другоеthe solvent was removed in vacuo
  11. 11
    workup.DISTILLATIONDistillation of the product at reduced pressure

Методика

Sodium metal (7.6 g, 0.33 g/atom) was dispersed in 50 ml of dry xylene (distilled from sodium hydride) by heating to 130° C. with rapid stirring. Dry xylene (168 ml) and 47.8 g (45.2 ml, 0.298 mole) of diethyl malonate were then added thereto and the mixture was allowed to react at 120° C. To the resultant mixture there was then added 48.1 g (0.116 mole) of 2-ethyl-propyl-1,3-ditosylate (prepared in 1B) dissolved in 120 ml of dry xylene. This reaction mixture was heated to about 150° C. and stirred for 18 hr. The mixture was cooled and poured into 500 ml of water and extracted with 600 ml (3×300 ml) of ether. The aqueous material was made acidic with 10% aqueous HCl and then extracted with 600 ml (2×300 ml) of ether. The combined ether extract was washed with 200 ml of saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and the solvent was removed in vacuo. Distillation of the product at reduced pressure yielded 7.0 g of the title compound having the following physical characteristics:

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04220795uspto-grants-1980_09