HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(3-chloro-4-fluorophenyl)-4-methyl-3-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-4-fluoroaniline | HCID 9708 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methyl-3-nitrobenzoyl chloride | HCID 66323 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-chloro-4-fluorophenyl)-4-methyl-3-nitrobenzamide | HCID 710855 | — |
Reaction Steps
To a solution of 4-methyl-3-nitrobenzoyl chloride (2.0 g) in dichloromethane (20 ml), a solution of triethylamine (0.7 ml) and 3-chloro-4-fluoroaniline (0.7 g) in dichloromethane (15 ml) was added dropwise in an ice-bath with the temperature no more than 5° C. After addition, the reaction was carried out for 30 min in an ice-bath, and then at room temperature overnight. The completion of reaction was indicated by TLC. Then potassium carbonate solution (10%) was added to precipitate a solid. The mixture was left to stand, and filtered. The filter cake was washed with water, and dried to give a pale yellow powdered solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426446B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-7821722097a148edac8e0ae6e5b8fd59 |
| Source note | uspto-grants-2013_04 |