Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,4,6-Trifluoro-3-(trifluoromethyl)benzoic acid | HCID 2777996 | — |
| Product | HCID 19035210 | HCID 19035210 | — |
Reaction Steps
5.8 g (0,024 mol) of 2,4,6-trifluoro-3-trifluoromethylbenzoic acid are added in portions at room temperature to 40 ml of thionyl chloride. After metering has ended, the mixture is heated at 50° C. until the evolution of gas has ceased. The excess thionyl chloride is then removed by distillation, and the crude product is reacted further directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05457104 |
|---|
| Source dataset | uspto-grants-1995_10 |
|---|
| ORD ID | ord-799914084c4b410cbd0f94c59343e7ce |
|---|
| Source note | uspto-grants-1995_10 |
|---|
