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Sodium Iodide → (R)-5-acetoxy-1-iodohexane

HRID 1421239
ノート
印刷プレビュー

反応式

HRID 1421239 の反応式
[C:1]([O:4][C@H:5]([CH3:11])[CH2:6][CH2:7][CH2:8][CH2:9]Cl)(=[O:3])[CH3:2].[I-:12].[Na+]>>[C:1]([O:4][C@H:5]([CH3:11])[CH2:6][CH2:7][CH2:8][CH2:9][I:12])(=[O:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 5238Sodium IodideHCID 110194345-(R)-Acetoxy-1-chlorohexane

生成物 1

HCID 54009360(R)-5-acetoxy-1-iodohexane

実験手順

First, (R)-5-acetoxy-1-iodohexane was prepared in the following manner. A solution of (R)-5-acetoxy-1-chlorohexane (4.80 g:26.89 mmol) was added to sodium iodide (5.39 g:36 mmol) in a round bottomed flask fitted with magnetic stirrer bar and a reflux condenser and refluxed for 12 hrs with stirring. Acetone was removed under reduced pressure, The crude product was partitioned between ethyl acetate (50 ml) and water layer (60 ml). The organic layer was washed with 10% sodium thiosulphate solution followed by water (20 l), dried over anhydrous Mg SO4 and concentrated under reduced pressure. Yield=7 g (96%)

後処理

  1. customfitted with magnetic stirrer bar and a reflux condenser
  2. temperaturerefluxed for 12 hrs
  3. customAcetone was removed under reduced pressure
  4. customThe crude product was partitioned between ethyl acetate (50 ml) and water layer (60 ml)
  5. washThe organic layer was washed with 10% sodium thiosulphate solution
  6. dry with materialdried over anhydrous Mg SO4
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-8023ee2153144af6bd5ffc00179b81c6
出典データセット
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06075029

反応ノート

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