Iodine → 4-Iodobiphenyl

HRID 1459680Notes

Reaction equation

HRID 1459680 reaction equation
C[Sn](Cl)(C)C.[Na].Br[C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:10][CH:9]=1.C[Sn](C)C.[I:24]I>COCCOC.CCOC(C)=O>[I:24][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:10][CH:9]=1

Participants

8

Conditions

Temperature
0 °C

Procedure

A solution of trimethyltin chloride (5.5 g, 27.60 mmoles) in 5 mL of DME was added to a stirred suspension of small cubes of metallic sodium (1.9 g, 82.64 mg atom) in 15 mL of DME under an argon stream in an ice bath. When the addition was complete, the mixture was stirred and chilled in an ice bath for 2 hrs. (the color changed to green). The mixture was cannulated into another dry and under argon round bottom flask to remove excess sodium and cooled to 0° C. A solution of 4-bromobiphenyl (5.4 g, 22.70 mmoles) in 14 mL of DME was added dropwise to the chilled NaSnMe3 solution. The resulting solution was stirred at room temperature overnight at which time TLC analysis showed complete reaction. Rf of the trimethyltin product=0.44 (silica, hexanes). The reaction mixture was then cooled in an ice bath and treated with iodine (6.6 g, 26.00 mmoles). After stirring at room temperature for 1.5 hrs, the mixture was diluted with EtOAc, washed with water, brine, dried over MgSO4, and the solvent removed at reduced pressure. The crude product was then purified by column chromatography with hexanes to afford 5.5 g (86% yield) of white solid.

Workup

  1. additionWhen the addition
  2. temperaturechilled in an ice bath for 2 hrs
  3. customanother dry and under argon round bottom flask
  4. customto remove excess sodium
  5. stirringThe resulting solution was stirred at room temperature overnight at which time TLC analysis
  6. customreaction
  7. temperatureThe reaction mixture was then cooled in an ice bath
  8. stirringAfter stirring at room temperature for 1.5 hrs
  9. washwashed with water, brine
  10. dry with materialdried over MgSO4
  11. customthe solvent removed at reduced pressure
  12. customThe crude product was then purified by column chromatography with hexanes

Sources & evidence

ORD record
ord-63e73f3a8dea4027a984a31151c4769c
Source dataset
uspto-grants-1998_12
Patent number
US05854277

Reaction notes

Loading…