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Trifluoroacetic acid → HCID 54076691、化合物

HRID 1471053
ノート
印刷プレビュー

反応式

HRID 1471053 の反応式
[C:1]([O:5][C:6]([NH:8][C@@H:9]([C:13]([O:16][CH3:17])([CH3:15])[CH3:14])[C:10]([OH:12])=[O:11])=[O:7])(C)(C)C.FC(F)(F)C(O)=O.[OH-].[Na+].ClC(OC)=O>C(Cl)Cl.CCOC(C)=O>[CH3:17][O:16][C:13]([CH3:15])([CH3:14])[C@H:9]([NH:8][C:6]([O:5][CH3:1])=[O:7])[C:10]([OH:12])=[O:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6422Trifluoroacetic acidHCID 6586Methyl chloroformateHCID 14798Sodium HydroxideHCID 59611493(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-methoxy-3-methylbutanoic acid

生成物 1

HCID 54076691HCID 54076691、化合物収率 71%

試薬・触媒・溶媒 2

HCID 6344
Dichloromethane
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of Example 203B (163 mg, 0.66 mmol) in CH2Cl2 (2 mL) was added trifluoroacetic acid (2 mL) and the solution was stirred at room temperature for 1 h. Solvent was removed in vacuo and the residue was suspended in saturated NaHCO3, extracted with EtOAc, the organic extracts combined, washed with brine, dried (Na2SO4), filtered and solvent removed in vacuo. The residue was dissolved in dioxane (1 mL) and 1 M NaOH (1.1 mL, 2.175 mmol) was added followed by the dropwise addition of methyl chloroformate (0.102 mL, 1.3 mmol). The solution was stirred at room temperature for 16 h, diluted with EtOAc, washed with 1 N HCl, brine, dried (Na2SO4), filtered and solvent removed in vacuo to give the title compound (96 mg, 0.468 mmol, 71%).

後処理

  1. customSolvent was removed in vacuo
  2. extractionextracted with EtOAc
  3. washwashed with brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. customsolvent removed in vacuo
  7. dissolutionThe residue was dissolved in dioxane (1 mL)
  8. stirringThe solution was stirred at room temperature for 16 h
  9. washwashed with 1 N HCl, brine
  10. dry with materialdried (Na2SO4)
  11. filtrationfiltered
  12. customsolvent removed in vacuo

出典と根拠

ORDレコード
ord-2e8cb32ec81b4ae38cf8c84dcaec61f7
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09006387B2

反応ノート

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