Boron trifluoride etherate → 1-Benzyl-4-(2-fluoro-5-methylbenzyl)piperidin-4-ol

HRID 270037

반응식

HRID 270037 반응식
Br[C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[F:9].[Li]CCCC.B(F)(F)F.CCOCC.[CH2:24]([N:31]1[CH2:38][CH2:37][C:34]2([O:36][CH2:35]2)[CH2:33][CH2:32]1)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>C1COCC1>[CH2:24]([N:31]1[CH2:38][CH2:37][C:34]([CH2:35][C:2]2[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=2[F:9])([OH:36])[CH2:33][CH2:32]1)[C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1

참가 물질

6

반응 조건

온도
-70 °C

실험 절차

To a solution of 2-bromo-1-fluoro-4-methylbenzene (0.76 g, 4 mmol) in THF (15 ml) at −70° C. under Ar a solution of n-BuLi (1.6 M in hexane, 2.5 ml, 4 mmol) was added dropwise. The reaction mixture was stirrred at −70° C. for 1 h, then BF3.Et2O (0.5 ml, 4 mmol) was added. After stirring for 20 min at −70° C., a solution of 6-benzyl-1-oxa-6-azaspiro[2.5]octane (0.41 g, 2 mmol) in dry THF (5 ml) was added dropwise. The stirring was continued for 2 h at −70° C., then the reaction mixture was quenched with sat. aq. NH4Cl (20 ml). The layers were separated, the aqueous layer extracted with THF. The combined organic layers were dried over Na2SO4. The solvent was removed in vacuo. Diethyl ether (50 ml) was added to the residue, folowed by a 2 M HCl in Et2O (5 ml). The precipitate was collected, washed with Et2O, and dissolved in minimal volume of methanol (ca. 5 ml). Water (50 ml) was added, and pH adjusted to 10 by addition of 2 M aq. NaOH. The mixture was extracted with ethyl acetate (2×25 ml), and the combined organic extracts were dried with Na2SO4. Evaporation of solvent afforded brownish oil.

후처리

  1. waitThe stirring was continued for 2 h at −70° C.
  2. customthe reaction mixture was quenched with sat. aq. NH4Cl (20 ml)
  3. customThe layers were separated
  4. extractionthe aqueous layer extracted with THF
  5. dry with materialThe combined organic layers were dried over Na2SO4
  6. customThe solvent was removed in vacuo
  7. additionDiethyl ether (50 ml) was added to the residue
  8. customThe precipitate was collected
  9. washwashed with Et2O
  10. dissolutiondissolved in minimal volume of methanol (ca. 5 ml)
  11. additionWater (50 ml) was added
  12. additionpH adjusted to 10 by addition of 2 M aq. NaOH
  13. extractionThe mixture was extracted with ethyl acetate (2×25 ml)
  14. dry with materialthe combined organic extracts were dried with Na2SO4
  15. customEvaporation of solvent
  16. customafforded brownish oil

출처 및 근거

ORD 기록
ord-150d93bae2494a3b807a6ae59d3dc564
출처 데이터셋
uspto-grants-2008_11
특허 번호
US07449475B2

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