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HRID 50152作成日:2026年10月24日

Biphenyl → Biphenyl

https://huagongshe.com/ja/reaction/50152

反応式

関与物質

役割名称HCID仕込み量
反応物BiphenylHCID 7095—
反応物4-ChlorobiphenylHCID 16323—
反応物ChlorineHCID 24526—
触媒IronHCID 23925—
溶媒ChlorobenzeneHCID 7964—
生成物BiphenylHCID 7095—
生成物3-ChlorobiphenylHCID 16322—
生成物4-ChlorobiphenylHCID 16323—
生成物2-ChlorobiphenylHCID 249266—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710217B1
出典データセットuspto-grants-2004_03
ORD IDord-ae882cb1dfff490a8f85983c7aca00aa
出典メモuspto-grants-2004_03