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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860356Generated: October 26, 2026

Iodine → 4-Ethyl-4'-iodobiphenyl

https://huagongshe.com/reaction/1860356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantOrthoperiodic acidHCID 25289—
Reactant4-EthylbiphenylHCID 79786—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product4-Ethyl-4'-iodobiphenylHCID 15477828—

Reaction Conditions

Temperature70 °C

Reaction Steps

25.0 g (137 mmol) of 4-ethylbiphenyl, 7.23 g (27.4 mmol) of orthoperiodic acid, 13.9 g (54.9 mmol) of iodine, 133 ml of acetic acid, 27 ml of water and 4.1 ml of sulfuric acid were placed in a 500 ml three-necked flask with a mechanical stirrer and bulb-shaped cooler. This was heated to 70° C. in a water bath, and subjected to the reaction for 2 hours. The product was cooled down to the ambient temperature. To this was added 300 ml of water, which was subjected to the extraction with chloroform. The resultant chloroform phase was washed with sodium thiosulfate and water in this order. To this was added sodium sulfate, and the dehydration was carried out. After the filtration was carried out, the chloroform was distilled away in an evaporator to obtain a light yellow solid. The resultant solid was recrystallized in the presence of ethanol to obtain a white crystal. The yield of the compound was 71%. Its melting point was 145-149° C. The IR chart is shown in FIG. 24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528657B2
Source datasetuspto-grants-2003_03
ORD IDord-5e84395f5d5244698bb30c6892a000d9
Source noteuspto-grants-2003_03