반응 #5695

ord-a27889ee44e040db9dcdb94b80457c09

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.DISSOLUTIONAll of the solid did not dissolve
  3. 3
    workup.WAITThe stirring was continued for 67.5 hours
  4. 4
    기타The layers were separated
  5. 5
    추출The aqueous layer was extracted with ether (2×75 ml)
  6. 6
    세척The combined ether phases were washed with 50 ml of brine
  7. 7
    건조dried over MgSO4
  8. 8
    기타Evaporation of the solvent
  9. 9
    workup.WAITleft 16.02 g of brown oil
  10. 10
    기타The oil was chromatographed on a 1100 g column of silica gel
  11. 11
    세척The column was eluted with 10% acetone-Skellysolve B and 2200 ml fractions
  12. 12
    기타were collected

실험 절차

To a solution of 2.39 g (9.04 mmoles) of 18-crown-6 in 250 ml of dry ether was added 13.1 g (116.7 mmoles) of potassium tert-butoxide. The mixture was stirred while 11.72 g (100 mmoles) indole was added. The stirring was continued for 3 hours. All of the solid did not dissolve. Then 14.1 g (116.5 mmoles) of allyl bromide in 100 ml of ether was added during 0.5 hour. The stirring was continued for 67.5 hours. Water (200 ml) was added. The layers were separated. The aqueous layer was extracted with ether (2×75 ml). The combined ether phases were washed with 50 ml of brine and dried over MgSO4. Evaporation of the solvent left 16.02 g of brown oil. The oil was chromatographed on a 1100 g column of silica gel. The column was eluted with 10% acetone-Skellysolve B and 2200 ml fractions were collected. The fractions were assayed by silica gel tlc (1×4") (10% acetone-Skellysolve B). Fractions 17-23 were combined giving 11.60 g (74%) of 1-allylindole as a yellow brown oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05245046uspto-grants-1993_09