Реакция #6653

ord-413684e85ed6442a83d777131c638b39

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe isopropanol was removed under vacuum
  2. 2
    ЭкстракцияThe residue was extracted with ether
  3. 3
    Экстракцияthe ether extract
  4. 4
    Промывкаwas washed successively with water and saturated NaCl solution
  5. 5
    Сушкаdried (MgSO4)
  6. 6
    ДругоеThe solvent was removed vacuo
  7. 7
    Другоеthe residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes)

Методика

To a solution of 569 mg (2.21 mmol) of 4,4-dimethyl-6-trimethylsilylethynyl-1,2,3,4-tetrahydroquinoline (Compound 95) in 3 ml of isopropanol was added, under argon, 1 ml of 1N aqueous KOH solution. The reaction mixture was stirred at room temperature for 36 h and the isopropanol was removed under vacuum. The residue was extracted with ether and the ether extract was washed successively with water and saturated NaCl solution and then dried (MgSO4). The solvent was removed vacuo and the residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes) to give the title compound as a brown oil. PMR (CDCl3): δ 1.26 (6H, s), 1.65-1.72 (2H, m), 2.96 (1H, s), 3.27-3.34 (2H, m), 6.34 (1H, d, J~8.3 Hz), 7.08 (1H, dd, J~8.3 Hz, 1.6 Hz), 7.33 (1H, d, J~1.6 Hz).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05248777uspto-grants-1993_09