HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Acifluorfen | HCID 44073 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chloride | HCID 3017765 | — |
Reaction Steps
2-Nitro-5-(2-chloro-4-trifluoromethylphenoxy)benzoic acid (80 grams) and toluene (80 ml) were charged into a reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. Thionyl chloride (80 ml) was slowly added at room temperature with stirring. After the addition was completed, the mixture was heated at reflux with continued stirring for a period of one hour. Stirring was thereafter continued at room temperature overnight. After this time the reaction mixture was stripped of toluene to yield the desired product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04618359 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-a4c4c3342db04ceb84c38365d763ccc8 |
| Source note | uspto-grants-1986_10 |