Реакция #2290316

ord-47a170b932204ece87c5c88b09c8970c

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.DISSOLUTIONwere dissolved
  2. 2
    ЭкстракцияThe reaction mixture was extracted with ethyl acetate (3×15 mL)
  3. 3
    Сушкаthe organic extracts were dried over sodium sulfate
  4. 4
    Фильтрацияfiltered
  5. 5
    Концентрированиеconcentrated
  6. 6
    Другоеdried overnight under vacuum

Методика

A solution of (S)-amino-(tetrahydro-pyran-4-yl)-acetic acid (1 g, 6.28 mmol) in saturated aqueous sodium bicarbonate solution (12.32 mL, 125.6 mmol) was stirred until all solids were dissolved. Methyl chloroformate (0.97 mL, 12.56 mmol) was added dropwise, the reaction mixture was stirred for 1 h, and IN HCl was added to adjust pH to 1. The reaction mixture was extracted with ethyl acetate (3×15 mL) and the organic extracts were dried over sodium sulfate, filtered, concentrated and dried overnight under vacuum to give the title intermediate (1.36 g, 99% yield) as a white, sticky solid. (m/z): [M+H]+ calcd for C9H15NO5 218.10 found 218.3.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09365549B2uspto-grants-2016_06