Реакция #416778

ord-8993049324244e9cab065f317b7a26b4

Растворители

Условия реакции

Температура
5°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONTo this mixture was added
  2. 2
    workup.ADDITIONwas added
  3. 3
    ДругоеAfter twenty hours the organic phase was separated
  4. 4
    Сушкаdried over anhydrous magnesium sulfate
  5. 5
    Концентрированиеconcentrated to an oil
  6. 6
    ДругоеThis oil was chromatographed on silica gel with 40% ethyl acetate-hexane

Методика

To a stirred mixture of 5.3 g (47 mmol) of N-isopropylhydroxylamine hydrochloride in 100 ml of methylene chloride cooled to 5° C. was added 3.8 g (47 mmol) of 50% sodium hydroxide solution in 20 ml of water. To this mixture was added with stirring 12.4 g (47 mmol) of 2,4-dibromobutyrylchloride and twenty minutes later an additional 7.6 g (94 mmol) of 50% sodium hydroxide solution was added. After twenty hours the organic phase was separated, dried over anhydrous magnesium sulfate and concentrated to an oil. This oil was chromatographed on silica gel with 40% ethyl acetate-hexane to afford 1.1 g of oily dihydro-4-bromo-2-isopropyl-2H-1,2-oxazin-3(4H)-one.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04892870uspto-grants-1990_01