Tetrahydrofuran → (4-{1-Ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl-phenyl]-propyl}-2-methyl-benzyloxy)-acetic acid

HRID 502066노트

반응식

HRID 502066 반응식
C[O:2][C:3](=[O:41])[CH2:4][O:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]([C:18]2[CH:23]=[CH:22][C:21]([O:24][CH2:25][CH:26]([O:31][Si](C(C)(C)C)(C)C)[C:27]([CH3:30])([CH3:29])[CH3:28])=[C:20]([CH3:39])[CH:19]=2)([CH2:16][CH3:17])[CH2:14][CH3:15])=[CH:9][C:8]=1[CH3:40].C1COCC1.CCCC[N+](CCCC)(CCCC)CCCC.[F-].[OH-].[Na+]>O>[CH2:14]([C:13]([C:10]1[CH:11]=[CH:12][C:7]([CH2:6][O:5][CH2:4][C:3]([OH:41])=[O:2])=[C:8]([CH3:40])[CH:9]=1)([C:18]1[CH:23]=[CH:22][C:21]([O:24][CH2:25][CH:26]([OH:31])[C:27]([CH3:29])([CH3:30])[CH3:28])=[C:20]([CH3:39])[CH:19]=1)[CH2:16][CH3:17])[CH3:15]

참가 물질

6

실험 절차

To a solution of enantiomer 1 of [4-(1-{4-[2-(tert-butyl-dimethyl-silanyloxy)-3,3-dimethyl-butoxy]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-benzyloxy]-acetic acid methyl ester (0.96 g, 1.64 mmol) and THF (10 mL) is added 1M TBAF (3.3 mL, 3.28 mmol). The solution is heated at a reflux overnight and concentrated. The residue is dissolved in MeOH (5 mL) and water (1 mL), NaOH (0.33 g, 8.21 mmol) is added and the solution is heated at reflux for 3 hours. The solution is concentration, dissolved in EtOAc (20 mL), washed with 1M HCl (15 mL), water (15 mL), brine (15 mL), dried over MgSO4, and concentrated. The residue is chromatographed to furnish the title compound (0.45 g, 0.99 mmol, 60%).

후처리

  1. temperatureThe solution is heated at a reflux overnight
  2. concentrationconcentrated
  3. dissolutionThe residue is dissolved in MeOH (5 mL)
  4. temperaturethe solution is heated
  5. temperatureat reflux for 3 hours
  6. concentrationconcentration
  7. dissolutiondissolved in EtOAc (20 mL)
  8. washwashed with 1M HCl (15 mL), water (15 mL), brine (15 mL)
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated
  11. customThe residue is chromatographed

출처 및 근거

ORD 기록
ord-c400e2a7f630406d925df63289c5bf5c
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07772425B2

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