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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603187Generated: November 1, 2026

Bromide ion → 5,5'-Dihydroxy-2,2'-diiodobiphenyl

https://huagongshe.com/reaction/1603187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantHydrogen BromideHCID 260—
ReactantBoron tribromideHCID 25134—
ReactantHCID 10895916HCID 10895916—
SolventDichloromethaneHCID 6344—
Product5,5'-Dihydroxy-2,2'-diiodobiphenylHCID 22625300—

Reaction Steps

The second 2,2'-dihalo-5,5'-dimethoxybiphenyl , and preferably 2,2'-diiodo-5,5'-dimethoxybiphenyl, is then demethylated under temperatures of about -78° C. to about -20° C., and preferably from about -78° C. to about -50° C., and ambient pressure, with a bromide-containing compound such as hydrogen bromide, boron tribromide, or mixtures thereof in a chlorinated solvent such as a chlorohydrocarbon including but not limited to dichloromethane to yield 2,2'-dihalo-5,5'-dihydroxybiphenyl, and preferably 2,2'-diiodo-5,5'-dihydroxybiphenyl. Boron tribromide is the preferred reactant. The concentration of the bromide-containing compound in the chlorinated solvent may range from 0.05M to about 1M, and preferably from about 0.1M to about 0.5M. The period of the demethylation reaction may depend upon the chemical structure, but will generally be from about 5 minutes to about 2 hours, and preferably from about 15 minutes to about 1 hour. The molar ratio of 2,2'-diiodo-5,5'dimethoxybiphenyl to the bromide-containing compound is about 1:3 to 1:10, and preferably about 1:2.5 to 1:5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05986045
Source datasetuspto-grants-1999_11
ORD IDord-b03a371cecc94e8ebf9db1942bf6b23e
Source noteuspto-grants-1999_11