HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 3,5-Bis(trifluoromethyl)chlorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Benzene, 1,3-bis(trifluoromethyl)- | HCID 223106 | — |
| Product | 3,5-Bis(trifluoromethyl)chlorobenzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04351975 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-1c39f0b0e3bf43ec819efe7bdeace7cc |
| Source note | uspto-grants-1982_09 |