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HRID 1703406作成日:2026年10月27日

Iodine → 3,5-Bis(trifluoromethyl)chlorobenzene

https://huagongshe.com/reaction/1703406

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物ChlorineHCID 24526—
反応物Chlorosulfonic acidHCID 24638—
反応物Benzene, 1,3-bis(trifluoromethyl)-HCID 223106—
生成物3,5-Bis(trifluoromethyl)chlorobenzeneHCID 2769405—

反応手順

130 parts of chlorosulfonic acid are introduced, at room temperature, into a reaction vessel, and 42.8 parts of 1,3-bis-(trifluoromethyl)-benzene and 2 parts of iodine are added. The suspension is cooled to 0° and 30 parts of chlorine are introduced in the course of 5 hours at 0° to 5°. The suspension is then poured out onto ice and the organic phase is separated from the aqueous phase. The organic phase is washed neutral with ice-cold water and is dried over calcined sodium sulfate. 38 parts of 5-chloro-1,3-bis-(trifluoromethyl)-benzene, of boiling point 111° to 112°, are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04351975
出典データセットuspto-grants-1982_09
ORD IDord-1c39f0b0e3bf43ec819efe7bdeace7cc
出典メモuspto-grants-1982_09