Potassium bis(trimethylsilyl)amide → Tert-butyl 3-(4-bromo-2-methylphenyl)pyrrolidine-1-carboxylate

HRID 503911노트

반응식

HRID 503911 반응식
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[Br:11][C:12]1[CH:17]=[CH:16][C:15]([CH:18]([CH2:26][NH:27][C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])[CH2:19][CH2:20]OS(C)(=O)=O)=[C:14]([CH3:35])[CH:13]=1>C1COCC1>[C:31]([O:30][C:28]([N:27]1[CH2:20][CH2:19][CH:18]([C:15]2[CH:16]=[CH:17][C:12]([Br:11])=[CH:13][C:14]=2[CH3:35])[CH2:26]1)=[O:29])([CH3:34])([CH3:33])[CH3:32]

참가 물질

4

실험 절차

KHMDS (0.5 M in toluene, 186 mL, 0.09303 mol) was added at 0° C. to methanesulfonic acid 3-(4-bromo-2-methyl-phenyl)-4-tert-butoxycarbonylamino-butyl ester (36.9 g, 0.08457 mol) dissolved in THF (400 mL). The ice-bath was removed and the mixture was stirred at room temperature for 2 hours. A saturated solution of NH4Cl was added to the reaction mixture and the resulting mixture was extracted with EtOAc. The combined organic extracts were washed with water and brine, dried over MgSO4, filtered, and evaporated under reduced pressure. The residue was purified via flash chromatography (hexane/EtOAc, 8/2) to give 27.3 g (95% yield) of 3-(4-bromo-2-methyl-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester as a clear oil.

후처리

  1. customThe ice-bath was removed
  2. additionA saturated solution of NH4Cl was added to the reaction mixture
  3. extractionthe resulting mixture was extracted with EtOAc
  4. washThe combined organic extracts were washed with water and brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated under reduced pressure
  8. customThe residue was purified via flash chromatography (hexane/EtOAc, 8/2)

출처 및 근거

ORD 기록
ord-115c77264bbc423fabf542c78282a3ce
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07776910B2

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