HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → (2-Chloro-6-fluorophenyl)-P-tolyl-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-N-(4-methylphenyl)acetamide | HCID 27967 | — |
| Reactant | 2-Chloro-6-fluorophenol | HCID 2773710 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-(2'-chloro-6'-fluorophenoxy)-N-(4-methylphenyl)acetamide | HCID 68956063 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | (2-Chloro-6-fluorophenyl)-P-tolyl-amine | HCID 21100364 | — |
Reaction Steps
14.65 g (100 mmol) of 2-chloro-6-fluorophenol are dissolved in 50 ml of 2-propanol followed by the addition of 15.5 g (112 mmol) of potassium carbonate and 18.9 g (103 mmol) of 2-chloro-N-(4-methylphenyl)acetamide. The mixture is refluxed for 4 hours. At this time, the formation of 2-(2′-chloro-6′-fluorophenoxy)-N-(4-methylphenyl)acetamide is completed. 20 ml of sodium methylate solution 30% in methanol are slowly added. To maintain a temperature of at least 75° C., about 25 ml of solvent are distilled during the addition. The mixture is boiled 2 hours more to complete the formation of (2′-chloro-6′-fluorophenyl)-(4-methylphenyl)-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07402603B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-fe3f4025b77d41a2bd8606edeb9df2fb |
| Source note | uspto-grants-2008_07 |