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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751322Generated: October 26, 2026

Iodine → 4-Bromo-4'-iodobiphenyl

https://huagongshe.com/reaction/1751322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-BromobiphenylHCID 7101—
ReactantIodic acidHCID 24345—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product4-Bromo-4'-iodobiphenylHCID 10904452325.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

A 4-neck one liter round bottom flask equipped with mechanical stirrer, thermometer and reflux condenser topped with nitrogen bubbler inlet was charged with 4-bromobiphenyl (23.31 g, 100 mmol) in acetic acid (400 mL), sulfuric acid (10 mL) and water (20 mL). To this stirring mixture was added iodic acid (4.84 g, 27.5 mmol) followed immediately by addition of iodine chips (11.17 g, 44.0 mmol). The reaction flask was immersed in a preheated tri(ethylene glycol) heating bath and heated at 65° C. internal temperature. After 30 min the bath temperature was increased such that the internal temperature raised to 85° C. after 20 min. Heating at this temperature was continued for 4.5 hours at which point UPLC analysis showed the reaction to be complete. After stirring overnight at room temperature the reaction mixture was vacuum filtered through a coarse fritted funnel and the solids were rinsed with water. The resulting white solid (32.1 g, 89% yield) had mp 177-179° C. and was used without further purification in the next step. NMR analysis confirmed the structure of Intermediate Compound 3,4-bromo-4′-iodobiphenyl. Purity (UPLC): >99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09159927B2
Source datasetuspto-grants-2015_10
ORD IDord-3520cd9a0e424b49811ac7d96feba9c5
Source noteuspto-grants-2015_10