HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 3-Chloro-2,4,5-trifluorobenzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Fuming sulfuric acid | HCID 24681 | — |
| Reactant | 2,4,5-Trifluorobenzoic acid | HCID 521170 | — |
| Product | 3-Chloro-2,4,5-trifluorobenzoic Acid | HCID 2734269 | — |
Reaction Steps
The chlorination of the 2,4,5-trifluorobenzoic acid is carried out in the melt, under pressure and/or in a solvent, for example chlorosulphonic acid or oleum, in the presence of halogen transfer agents, for example iodine. 2,4,5-Trifluoro-3-chlorobenzoic acid is obtained in this reaction. However, since the reaction mixture still contains unchanged starting material and some 2,4,5,-trifluoro-3,6-dichlorobenzoic acid, the crude mixture is treated, without intermediate isolation, with thionyl chloride. The desired 2,4,5-trifluoro-3-chlorobenzoyl chloride is then obtained by fractional distillation. However, it is more favorable to carry out the separation by distillation of the acid fluorides.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05530158 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-83b9fe0250ff4251899db0af7444937c |
| Source note | uspto-grants-1996_06 |