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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722412Generated: October 25, 2026

3-Fluoro-4-nitroaniline → Cyclohexyl-n-(3-fluoro-4-nitrophenyl)carboxamide

https://huagongshe.com/reaction/722412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-nitroanilineHCID 75401—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
ProductCyclohexyl-n-(3-fluoro-4-nitrophenyl)carboxamideHCID 5874260080.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138420B2
Source datasetuspto-grants-2006_11
ORD IDord-742fac2e64c547abbb39b88fb01a7247
Source noteuspto-grants-2006_11