Imidazole → 4-(4-(Tert-butyldimethylsilyloxy)phenyl)-4-(2-fluorophenyl)cyclohexanone

HRID 2174434노트

반응식

HRID 2174434 반응식
N1C=CN=C1.[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]1([C:20]2[CH:25]=[CH:24][C:23]([OH:26])=[CH:22][CH:21]=2)[CH2:18][CH2:17][C:16](=[O:19])[CH2:15][CH2:14]1.[CH3:27][C:28]([Si:31](Cl)([CH3:33])[CH3:32])([CH3:30])[CH3:29].C([O-])(O)=O.[Na+]>CN(C=O)C>[Si:31]([O:26][C:23]1[CH:22]=[CH:21][C:20]([C:13]2([C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=3[F:6])[CH2:14][CH2:15][C:16](=[O:19])[CH2:17][CH2:18]2)=[CH:25][CH:24]=1)([C:28]([CH3:30])([CH3:29])[CH3:27])([CH3:33])[CH3:32]

참가 물질

6

실험 절차

Imidazole (128 mg, 1.9 mmol) was added to a solution of 6 (214 mg, 0.75 mmol) and TBDMSCl (136 mg, 0.90 mmol) in DMF (8 mL). The mixture was stirred at room temperature overnight. NaHCO3 (10 mL, saturated aqueous solution) was added and the mixture was extracted with EtOAc (2×40 mL). The combined organic phase was dried over Na2SO4 and the solvent was evaporated under reduced pressure. The concentrate was dissolved in EtOAc (50 mL) and the solution was washed with MgSO4 (4% aqueous solution). The organic phase was dried over Na2SO4, filtered and the solvent was evaporated under reduced pressure. Yield of crude: 394 mg (>100%) as a thick oil.

후처리

  1. extractionthe mixture was extracted with EtOAc (2×40 mL)
  2. dry with materialThe combined organic phase was dried over Na2SO4
  3. customthe solvent was evaporated under reduced pressure
  4. dissolutionThe concentrate was dissolved in EtOAc (50 mL)
  5. washthe solution was washed with MgSO4 (4% aqueous solution)
  6. dry with materialThe organic phase was dried over Na2SO4
  7. filtrationfiltered
  8. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-be7b3c33f41046fc9b1d88f06d467e4e
출처 데이터셋
uspto-grants-2015_06
특허 번호
US09061981B2

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