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Water → ethyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-hydroxypropanoate

HRID 72308
ノート
印刷プレビュー

反応式

HRID 72308 の反応式
[NH:1]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[C@H:2]([C:5]([OH:7])=[O:6])[CH2:3][OH:4].C([O-])([O-])=O.[K+].[K+].[CH2:21](I)[CH3:22].O>CN(C=O)C>[C:8]([NH:1][C@H:2]([C:5]([O:7][CH2:21][CH3:22])=[O:6])[CH2:3][OH:4])([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 98766N-[tert-butoxycarbonyl]-L-serine

生成物 1

HCID 13819295ethyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-hydroxypropanoate

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of Boc-Ser-OH (0.3 g, 1.46 mmol, 1 eq) in dry DMF (4 ml) at 0° C., dry K2CO3 (0.22 g, 1.6 mmol, 1.1 eq) was added. The resulting white suspension was stirred for 15 minute and ethyl iodide (0.68 g, 0.35 ml, 4.38 mmol, 3 eq) was dropwise added. The cooling was removed and reaction mixture was stirred at room temperature under N2 for 24 h. To the formed white emulsion H2O was added, and the mixture extracted by EtOAc. The combined organic layer was washed by H2O and then brine, and dried over MgSO4. The solvent was evaporated and the obtained oil was dried overnight in high vacuum. Yield of the pure F—0.27 g (79%).

後処理

  1. customThe cooling was removed
  2. customreaction mixture
  3. stirringwas stirred at room temperature under N2 for 24 h
  4. extractionthe mixture extracted by EtOAc
  5. washThe combined organic layer was washed by H2O
  6. dry with materialbrine, and dried over MgSO4
  7. customThe solvent was evaporated
  8. customthe obtained oil was dried overnight in high vacuum

出典と根拠

ORDレコード
ord-5f047d3589634eab8b0854184cd30d04
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08828993B2

反応ノート

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