Реакция #56083

ord-c6a2abd0262b46a8b5b77f566213ccef

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed with dilute hydrochloric acid
  2. 2
    Экстракцияextracted with an aqueous solution of 5% sodium hydrogen carbonate
  3. 3
    Экстракцияextracted with ethyl acetate
  4. 4
    ПромывкаThe extract is washed with water
  5. 5
    Другоеdried
  6. 6
    Другоеevaporated
  7. 7
    ДругоеThe residue is recrystallized from a mixture of ethyl acetate and ether

Методика

To a solution of benzyl 7β-(α-phenyl-α-carbobenzoxyaminoacetamido)-3-chloro-3-cephem-4-carboxylate (295 mg) in methylene chloride (6 ml) is added a solution of aluminum chloride (267 mg) in nitromethane (3 ml) under ice cooling. After stirring for 2 hours at room temperature, the mixture is diluted with ethyl acetate, washed with dilute hydrochloric acid, and extracted with an aqueous solution of 5% sodium hydrogen carbonate. The extract is acidified with hydrochloric acid and extracted with ethyl acetate. The extract is washed with water, dried, and evaporated. The residue is recrystallized from a mixture of ethyl acetate and ether to give 7β-(α-phenyl-glycinamido)-3-chloro-3-cephem-4-carboxylic acid (167 mg). Yield: 91.4%.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04223132uspto-grants-1980_09