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Sodium Iodide → Methyl (S)-2-(Boc-amino)-4-iodobutanoate

HRID 1715636
ノート
印刷プレビュー

反応式

HRID 1715636 の反応式
[CH3:1][O:2][C:3](=[O:16])[C@@H:4]([NH:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:6]Br.[Na+].[I-:18]>CC(C)=O>[CH3:1][O:2][C:3](=[O:16])[C@@H:4]([NH:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:6][I:18]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 5238Sodium IodideHCID 10685328Methyl (S)-2-(Boc-amino)-4-bromobutyrate

生成物 1

HCID 14394150Methyl (S)-2-(Boc-amino)-4-iodobutanoate収率 92%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

反応条件

温度
70 °C

実験手順

A mixture of (S)-4-bromo-2-tert-butoxycarbonylaminobutyric acid methyl ester (1.19 g, 4.0 mmol) (Example 120, Steps A-D) and NaI (6.0 g, 40.0 mmol) in acetone (25 mL) was heated to 70° C. for 2 hours. The mixture was then cooled to room temperature, concentrated under reduced pressure and partitioned between water (10 mL) and ether (40 mL). The layers were separated and the organic layer was washed with water (10 mL), dried over MgSO4, filtered through Celite, and concentrated under reduced pressure to afford 1.26 g of the product (92% yield).

後処理

  1. temperatureThe mixture was then cooled to room temperature
  2. concentrationconcentrated under reduced pressure
  3. custompartitioned between water (10 mL) and ether (40 mL)
  4. customThe layers were separated
  5. washthe organic layer was washed with water (10 mL)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered through Celite
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-72608d66019440e6900203f19c2d1e8c
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07799782B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート