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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703406Generated: October 25, 2026

Iodine → 3,5-Bis(trifluoromethyl)chlorobenzene

https://huagongshe.com/reaction/1703406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantChlorineHCID 24526—
ReactantChlorosulfonic acidHCID 24638—
ReactantBenzene, 1,3-bis(trifluoromethyl)-HCID 223106—
Product3,5-Bis(trifluoromethyl)chlorobenzeneHCID 2769405—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351975
Source datasetuspto-grants-1982_09
ORD IDord-1c39f0b0e3bf43ec819efe7bdeace7cc
Source noteuspto-grants-1982_09