HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477113Generated: October 29, 2026
N-Methylcyclohexylamine → HCID 52438095, compound
https://huagongshe.com/reaction/1477113
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 2,5-Difluoronitrobenzene | HCID 67767 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 52438095 | HCID 52438095 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403773B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-9391cd6ee90440fc969d614421b66f3e |
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| Source note | uspto-grants-2016_08 |
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