Iodine → 4-Iodobiphenyl
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]=1Participants
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
- additionWhen the addition
- temperaturechilled in an ice bath for 2 hrs
- customanother dry and under argon round bottom flask
- customto remove excess sodium
- stirringThe resulting solution was stirred at room temperature overnight at which time TLC analysis
- customreaction
- temperatureThe reaction mixture was then cooled in an ice bath
- stirringAfter stirring at room temperature for 1.5 hrs
- washwashed with water, brine
- dry with materialdried over MgSO4
- customthe solvent removed at reduced pressure
- 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
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