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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783889Generated: October 29, 2026

Cyclohexanemethylamine → Methyl {4-[(cyclohexylmethyl)amino]-3-nitrophenyl}carbamate

https://huagongshe.com/reaction/1783889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanemethylamineHCID 76688—
ReactantMethyl (4-fluoro-3-nitrophenyl)carbamateHCID 3636899—
SolventEthanolHCID 702—
ProductMethyl {4-[(cyclohexylmethyl)amino]-3-nitrophenyl}carbamateHCID 57591003—

Reaction Steps

Methyl(4-fluoro-3-nitrophenyl)carbamate (1.00 g, 4.67 mmol) and cyclohexylmethyl amine (0.730 mL, 5.60 mmol) were stirred in EtOH (20 mL) containing TEA (1.0 mL, 7.00 mmol) at 75° C. for 24 h. The solvent was concentrated. The residue was dissolved in EtOAc and washed with 5% KHSO4 aqueous solution, saturated NaHCO3 aqueous solution, brine and dried over anhydrous MgSO4. The crude product was purified by flash chromatography using 4:1/hexanes:EtOAc on silica gel. Yield: 1.05 g (73%); 1H NMR (400 MHz, CHLOROFORM-D) δ 1.04 (m, 2H), 1.25 (m, 3H), 1.69 (m, 2H), 1.77 (m, 2H), 1.83 (m, 1H), 1.86 (m, 1H), 3.14 (m, 2H), 3.78 (s, 3H), 6.46 (m, 1H), 6.84 (d, J=9.37, 1H), 7.63 (m, 1H), 8.05 (d, J=2.54 Hz, 1H), 8.09 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501447B2
Source datasetuspto-grants-2009_03
ORD IDord-b7cdc726aa8545ffacfb760efffc8f3b
Source noteuspto-grants-2009_03