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HRID 50152생성일: 2026년 10월 23일

Biphenyl → Biphenyl

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

반응식

참여 물질

역할이름HCID투입량
반응물BiphenylHCID 7095—
반응물4-ChlorobiphenylHCID 16323—
반응물ChlorineHCID 24526—
촉매IronHCID 23925—
용매ChlorobenzeneHCID 7964—
생성물BiphenylHCID 7095—
생성물3-ChlorobiphenylHCID 16322—
생성물4-ChlorobiphenylHCID 16323—
생성물2-ChlorobiphenylHCID 249266—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710217B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-ae882cb1dfff490a8f85983c7aca00aa
출처 메모uspto-grants-2004_03