Hydrochloric Acid → HCID 42622954、化合物

HRID 1092447ノート

反応式

HRID 1092447 の反応式
C([O:4][C@H:5]1[C@H:10]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[C:13]([CH2:18][C:19]3[CH:24]=[CH:23][C:22]([CH2:25][CH3:26])=[CH:21][CH:20]=3)[CH:12]=2)[C@@H:9]([O:27]C(=O)C)[C@H:8]([CH2:31][O:32]C(=O)C)[C@@H:7]([O:36]C(=O)C)[C@@H:6]1[O:40]C(=O)C)(=O)C.[OH-].[Na+].Cl>CO>[Cl:17][C:14]1[CH:15]=[CH:16][C:11]([C@@H:10]2[C@@H:9]([OH:27])[C@H:8]([CH2:31][OH:32])[C@@H:7]([OH:36])[C@H:6]([OH:40])[C@H:5]2[OH:4])=[CH:12][C:13]=1[CH2:18][C:19]1[CH:20]=[CH:21][C:22]([CH2:25][CH3:26])=[CH:23][CH:24]=1

参加物

5

実験手順

To a stirred solution of (1S,2R,3R,4S,5R,6R)-4-(acetoxymethyl)-6-(4-chloro-3-(4-ethylbenzyl)phenyl)cyclohexane-1,2,3,5-tetrayl tetraacetate (98 g, >99%, 0.158 mol, 1 eq) in methanol (1 L) was added sodium hydroxide (powder, 12.6 g, 0.315 mol, 2 eq) and the mixture was refluxed overnight. The mixture was acidified to pH 6 with 1 N hydrochloric acid and the volatiles were removed under reduced pressure. The residues were dissolved in ethyl acetate (3 L), washed with water (1 L), then with brine (1 L), dried over sodium sulfate, filtered and concentrated to give a white foam. The foam was recrystallized in refluxing ethanol/water (v/v=1:3, 20 mL/g (crude)) twice to give a white solid (58 g, purity of 99.3%, yield 90%).

後処理

  1. temperaturethe mixture was refluxed overnight
  2. customthe volatiles were removed under reduced pressure
  3. dissolutionThe residues were dissolved in ethyl acetate (3 L)
  4. washwashed with water (1 L)
  5. dry with materialwith brine (1 L), dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto give a white foam
  9. customThe foam was recrystallized
  10. temperaturein refluxing ethanol/water (v/v=1:3, 20 mL/g (crude)) twice
  11. customto give a white solid (58 g, purity of 99.3%, yield 90%)

出典と根拠

ORDレコード
ord-4eb9a5d06fed43018fc5a07fd6c65644
出典データセット
uspto-grants-2012_03
特許番号
US08129434B2

反応ノート

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