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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167446Generated: October 31, 2026

N-Methylcyclohexylamine → HCID 52438095, compound

https://huagongshe.com/reaction/2167446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant2,5-DifluoronitrobenzeneHCID 67767—
SolventWaterHCID 962—
ProductHCID 52438095HCID 5243809589%

Reaction Conditions

Temperature100 °C

Reaction Steps

Potassium carbonate (6.0 g, 43.5 mmol) and N-methylcyclohexylamine (4.6 g, 40.6 mmol) were added to a N-methylpyrolidone (NMP) solution (20 ml) of 2,5-difluoronitrobenzene (5.0 g, 31.4 mmol), and stirred at 100° C. for 3 hours. The reaction mixture was cooled to room temperature, water was added, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with water, and then dried over anhydrous magnesium sulfate. The resulting dry product was concentrated under reduced pressure to thereby obtain 7.0 g of oily yellow N-cyclohexyl-4-fluoro-2-nitro-N-methylaniline (yield: 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045464B2
Source datasetuspto-grants-2015_06
ORD IDord-754f22ab82bb4169b5dee5d937b4b408
Source noteuspto-grants-2015_06