Реакция #2348469

ord-c93a3c5a5b41463ea504659dc142aa7c

Растворители

Условия реакции

Температура
70°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction mixture was cooled to room temperature
  2. 2
    workup.STIRRINGThe mixture was stirred at room temperature for 18 hours
  3. 3
    Экстракцияthe reaction mixture was extracted with ethyl acetate
  4. 4
    ПромывкаThe extract was washed with aqueous saturated sodium chloride
  5. 5
    Сушкаdried over anhydrous sodium sulfate
  6. 6
    Концентрированиеconcentrated under reduced pressure

Методика

4.49 g of 2,2-dimethyl-6-(tetrahydro-2H-pyran-2-yloxy)-4-hexyn-3-one was dissolved in 20 ml of methanol, and 1.30 g of sodium methoxide and 1.53 g of hydroxylamine hydrochloride were added. The mixture was stirred at 70° C. for 2 hours. The reaction mixture was cooled to room temperature and then adjusted to pH 2 with concentrated hydrochloric acid. The mixture was stirred at room temperature for 18 hours. After aqueous saturated sodium hydrogen carbonate was added, the reaction mixture was extracted with ethyl acetate. The extract was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.12 g of (3-t-butyl-isoxazol-5-yl)methanol.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07846956B2uspto-grants-2010_12