Реакция #319542

ord-242e581e95754b6f8fb4fa6b1829b13a

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe mixture was filtered
  2. 2
    Другоеthe filtrate was evaporated
  3. 3
    ЭкстракцияThe residue was extracted twice with 250 ml of hot ethyl acetate each time
  4. 4
    Другоеthe combined ethyl acetate extracts were evaporated
  5. 5
    ДругоеThe residue was chromatographed on a short column of silica gel
  6. 6
    Промывкаfor the elution
  7. 7
    Другоеthe product was crystallized from a mixture of ethyl acetate and hexane

Методика

A solution of 2.50 g of 2',3'-dideoxy-5-ethyl-3'-iodouridine in a mixture of 90 ml of ethanolic ammonia and 17 ml of water was hydrogenated over 5% palladium on barium sulfate catalyst at room temperature and under atmospheric pressure for 3 hours. The mixture was filtered and the filtrate was evaporated. The residue was extracted twice with 250 ml of hot ethyl acetate each time and the combined ethyl acetate extracts were evaporated. The residue was chromatographed on a short column of silica gel using ethyl acetate for the elution and the product was crystallized from a mixture of ethyl acetate and hexane to give 1.17 g of 2',3'-dideoxy-5-ethyluridine in the form of a white solid of melting point 109°-113° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04851519uspto-grants-1989_07