HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluoro-4-nitroaniline → Cyclohexyl-n-(3-fluoro-4-nitrophenyl)carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluoro-4-nitroaniline | HCID 75401 | — |
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Product | Cyclohexyl-n-(3-fluoro-4-nitrophenyl)carboxamide | HCID 58742600 | 80.7% |
Reaction Steps
3-Fluoro-4-Nitroaniline (1 mmol, 0.15 g) was dissolved in a 3:1 mixture of CH2Cl2/THF (4 mL) and pyridine (0.2 mL) was added to the mixture, which was cooled in an ice-water bath under nitrogen. Cyclohexanecarbonylchloride (1.1 mmol, 0.162 g) was dissolved in CH2Cl2 (1 mL) and added dropwise to the above solution at 4° C. and stirred at room temperature for 3 h. The reaction mixture was diluted with CH2Cl2 (50 mL) and washed with 1N HCl, 10% NaHCO3, brine and water, dried over Na2SO4 and the solvent evaporated to afford cyclohexyl-N-(3-fluoro-4-nitrophenyl)carboxamide (0.215 g) of product (Yield: 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138420B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-742fac2e64c547abbb39b88fb01a7247 |
| Source note | uspto-grants-2006_11 |