HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(3-chloro-4-trifluoromethoxyphenyl)-1-methylcyclopropanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-4-(trifluoromethoxy)aniline | HCID 2773843 | — |
| Reactant | 1-Methylcyclopropane-1-carbonyl chloride | HCID 12789939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-chloro-4-trifluoromethoxyphenyl)-1-methylcyclopropanecarboxamide | HCID 13314711 | 89.2% |
Reaction Steps
To a solution of 3-chloro-4-trifluoromethoxyaniline (2.1 g) in methylene chloride (50 ml), triethylamine (1.1 g) was added, and a solution of 1-methylcyclopropanecarbonyl chloride (1.2 g) in methylene chloride was dropwise added thereto while stirring and ice-cooling. After stirring at room temperature for 1 hour, the reaction mixture was washed with 1 N hydrochloric acid, sodium hydrogen carbonate solution and saturated sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated. The crude crystals (2.9 g) were recrystallized from ethanol to give N-(3-chloro-4-trifluoromethoxyphenyl)-1-methylcyclopropanecarboxamide (2.6 g). M.P., 101°-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04447260 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-faa184fb958d49239921cbe6c9a76367 |
| Source note | uspto-grants-1984_05 |