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

HRID 1421239Notes

Reaction equation

HRID 1421239 reaction equation
[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]

Participants

3

Procedure

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%)

Workup

  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

Sources & evidence

ORD record
ord-8023ee2153144af6bd5ffc00179b81c6
Source dataset
uspto-grants-2000_06
Patent number
US06075029

Reaction notes

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