HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2,4-Dichloro-3-cyano-5-fluorobenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,4-Dichloro-3-cyano-5-fluorobenzoic acid | HCID 10900541 | — |
| Reactant | Hydrogen chloride sulphur dioxide | HCID 22338718 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2,4-Dichloro-3-cyano-5-fluorobenzoyl chloride | HCID 14300131 | 95.7% |
Reaction Steps
4100 ml of thionyl chloride and 41 ml of pyridine were introduced into a stirred apparatus fitted with metering device and gas outlet leading to a scrubber via a reflux condenser, and, at 20° C., 2050 g of 3-cyano-2,4-dichloro-5-fluorobenzoic acid (99.5% strength) were introduced at the rate of hydrogen chloride/sulphur dioxide evolution. At the end of the addition, the mixture was heated to reflux until the evolution of gas ceased. The mixture was then distilled. In the boiling range from 142 to 145° C./10 mbar, 2150 g (95.7% of theory) of 3-cyano-2,4-dichloro-5-fluorobenzoyl chloride were obtained (content according to GC: 98.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706918B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-db20833cfd08478986e3edb813feb9a4 |
| Source note | uspto-grants-2004_03 |