반응 #6083

ord-a5874430b1694beea4c83d85fd26590c

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Absolute ethanol was degassed
  2. 2
    기타the solvent removed in vacuo
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in water
  4. 4
    추출extracted with 50 ml ether, which
  5. 5
    추출extracted with 4×50 ml ether
  6. 6
    세척washed with water, saturated NaCl solution
  7. 7
    건조dried (MgSO4)
  8. 8
    기타Solvent was removed in vacuo

실험 절차

Absolute ethanol was degassed by applying a vacuum while simultaneously bubbling nitrogen through it. A solution of 188 mg (0.5201 mmol) ethyl 6-[2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronapth-2-yl)ethynyl]-nicotinoate in 2 ml absolute ethanol was treated with 800 ml of a 1.65M (1.32 mmol) solution of potassium hydroxide in ethanol and water. The mixture was stirred at room temperature for 18 hours and then the solvent removed in vacuo. The residue was dissolved in water and extracted with 50 ml ether, which was discarded. The aqueous layer was then acidified with glacial acetic acid and extracted with 4×50 ml ether. The ether extracts were combined, washed with water, saturated NaCl solution and then dried (MgSO4). Solvent was removed in vacuo to give the title compound as a pale yellow solid. PMR (CDCl3): δ1.31 (12 H, s), 1.71(4 H, s), 7.34 (1 H, d, J~7.8 Hz), 7.40 (1 H, d, J~7.8 Hz), 7.62 (1 H, s), 8.39 (1 H, dd, J~7.3 Hz, 2.1 Hz), 9.33 (1 H, d, J~2.1 Hz).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05246962uspto-grants-1993_09