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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50152Generated: October 27, 2026

Biphenyl → Biphenyl

https://huagongshe.com/reaction/50152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBiphenylHCID 7095—
Reactant4-ChlorobiphenylHCID 16323—
ReactantChlorineHCID 24526—
CatalystIronHCID 23925—
SolventChlorobenzeneHCID 7964—
ProductBiphenylHCID 7095—
Product3-ChlorobiphenylHCID 16322—
Product4-ChlorobiphenylHCID 16323—
Product2-ChlorobiphenylHCID 249266—

Reaction Steps

It would be desirable to be able to prepare 4-chlorobiphenyl in a single step from biphenyl and chlorine. According to U.S. Pat. No. 1,890,427, this is possible by chlorination of biphenyl in chlorobenzene in the presence of metallic iron as catalyst. However, this gives a mixture comprising 4-chlorobiphenyl, 3-chlorobiphenyl, 2-chlorobiphenyl and unreacted biphenyl. The separation of this mixture is very complicated. For separating off one isomer, the reference describes crystallization from noneutectic mixtures above the freezing point of the eutectic. This means that separation of the entire mixture makes it necessary to carry out a complicated sequence of distillation and crystallization steps. Czech. Chem. Prum., 30(10), 529-32 (1980) confirms this. To achieve purities of greater than 99%, the latter reference describes the following steps to be carried out in succession for the separation of mixtures comprising 2-, 3- and 4-chlorobiphenyl: 1. distillation, 2. crystallization of the fractions from the distillation and 3. recrystallization of the fractions from the crystallization from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710217B1
Source datasetuspto-grants-2004_03
ORD IDord-ae882cb1dfff490a8f85983c7aca00aa
Source noteuspto-grants-2004_03