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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459680Generated: November 1, 2026

Iodine → 4-Iodobiphenyl

https://huagongshe.com/reaction/1459680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-BromobiphenylHCID 7101—
ReactantTrimethyltin chlorideHCID 14016—
ReactantStannyl, trimethyl-HCID 5358116—
ReactantSodiumHCID 5360545—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product4-IodobiphenylHCID 1532286.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854277
Source datasetuspto-grants-1998_12
ORD IDord-63e73f3a8dea4027a984a31151c4769c
Source noteuspto-grants-1998_12