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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1703406Erstellt: 26. Oktober 2026

Iodine → 3,5-Bis(trifluoromethyl)chlorobenzene

https://huagongshe.com/reaction/1703406

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktChlorineHCID 24526—
EduktChlorosulfonic acidHCID 24638—
EduktBenzene, 1,3-bis(trifluoromethyl)-HCID 223106—
Produkt3,5-Bis(trifluoromethyl)chlorobenzeneHCID 2769405—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04351975
Quelldatensatzuspto-grants-1982_09
ORD IDord-1c39f0b0e3bf43ec819efe7bdeace7cc
Quellennotizuspto-grants-1982_09