Hydrochloric Acid → [(R)-1-hydroxymethyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl ester

HRID 12584

반응식

HRID 12584 반응식
[C:1]([O:5][C:6](=[O:21])[NH:7][C@:8]([CH2:19][OH:20])([CH3:18])[CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1)([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].[CH2:28](OS(C)(=O)=O)[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34].Cl>C(O)C.CCOC(C)=O>[C:1]([O:5][C:6](=[O:21])[NH:7][C@:8]([CH2:19][OH:20])([CH3:18])[CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])=[CH:13][CH:12]=1)([CH3:4])([CH3:2])[CH3:3]

참가 물질

7

실험 절차

To a stirred solution of [(R)-1-hydroxymethyl-3-(4-hydroxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl ester (2.06 g, 6.98 mMol) in ethanol (100 ml) is added potassium carbonate (2.90 g, 20.8 mMol) and methanesulfonic acid heptyl ester (2.04 g, 10.5 mMol). The mixture is heated to reflux temperature and stirred at that temperature for 6 hours. The mixture is then cooled to RT and stirred at RT overnight. The reaction mixture is then poured onto a biphasic mixture of AcOEt and HCl (aqueous, 1 M). The aqueous phase is extracted twice with AcOEt. The combined organic layers are washed with NaHCO3 (saturated aqueous solution), dried (Na2SO4) and concentrated under reduced pressure. Column chromatography eluting with 8% AcOEt in toluene gives the title compound as a colourless oil.

후처리

  1. temperatureThe mixture is heated
  2. temperatureto reflux temperature
  3. stirringstirred at RT overnight
  4. extractionThe aqueous phase is extracted twice with AcOEt
  5. washThe combined organic layers are washed with NaHCO3 (saturated aqueous solution)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated under reduced pressure
  8. washColumn chromatography eluting with 8% AcOEt in toluene

출처 및 근거

ORD 기록
ord-70054e6b95a147cabccc72cb3935270a
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07728020B2

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