Sodium Iodide → (4-Iodobutyl)benzene

HRID 342736Notes

Reaction equation

HRID 342736 reaction equation
[I-:1].[Na+].[C:3]1([CH2:9][CH2:10][CH2:11][CH2:12]Cl)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>CC(C)=O>[C:3]1([CH2:9][CH2:10][CH2:11][CH2:12][I:1])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Participants

4

Conditions

Temperature
70 °C

Procedure

Sodium iodide (8.9 g, 59.2 mol) and 4-phenyl-1-chlorobutane (5.0 g, 29.6 mol) were added to acetone (29.6 mL) at rt. The mixture was heated to 70° C. for 12 h. The resulting solution was gravity filtered to remove salts. The solvent was removed under reduced pressure and excess salts were dissolved in water (100 mL). Hexane (100 mL) was added to the aqueous mixture. The phases were separated and the organic phase was washed with saturated sodium bisulfite solution (3×50 mL), treated with decolorizing carbon, and gravity filtered. The organic layer was then dried (MgSO4), filtered, and concentrated in vacuo to afford 4-phenyl-1-iodobutane (6.94 g, 90%).

Workup

  1. filtrationfiltered
  2. customto remove salts
  3. customThe solvent was removed under reduced pressure and excess salts
  4. dissolutionwere dissolved in water (100 mL)
  5. additionHexane (100 mL) was added to the aqueous mixture
  6. customThe phases were separated
  7. washthe organic phase was washed with saturated sodium bisulfite solution (3×50 mL)
  8. additiontreated with decolorizing carbon, and gravity
  9. filtrationfiltered
  10. dry with materialThe organic layer was then dried (MgSO4)
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-fb5116ffbb5b42b792d1f70cfc24df3a
Source dataset
uspto-grants-1999_01
Patent number
US05859047

Reaction notes

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