Реакция #320288

ord-139b224165174673a406045bcf5d1011

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеconcentrated in vacuo
  2. 2
    Другоеpartitioned between EtOAc and 1 ml of water
  3. 3
    ЭкстракцияThe aqueous layer was extracted with EtOAc
  4. 4
    Сушкаthe organic layer was dried over Na2SO4
  5. 5
    Концентрированиеconcentrated in vacuo

Методика

To a suspension of 0.30 g (0.87 mmol) of ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate (Compound 1) in 4 ml of THF and 2 ml of ethanol was added 2 ml (2 mmol) of LiOH (1N aqueous solution). The reaction mixture was stirred at room temperature for 4 hours, concentrated in vacuo to near dryness, partitioned between EtOAc and 1 ml of water and acidified to pH 4 with 10% HCl. The aqueous layer was extracted with EtOAc and then the organic layer was dried over Na2SO4 and concentrated in vacuo to give the title compound as a light yellow solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05591858uspto-grants-1997_01