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

HRID 1421239
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1421239
[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]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

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

Produkt 1

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

Versuchsvorschrift

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%)

Aufarbeitung

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

    ORD-Eintrag
    ord-8023ee2153144af6bd5ffc00179b81c6
    Quelldatensatz
    uspto-grants-2000_06
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US06075029

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