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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51859Generated: October 26, 2026

Urea → Benzenamine, 4-methoxy-3-nitro-

https://huagongshe.com/reaction/51859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantP-AnisidineHCID 7732—
ReactantSodium HydroxideHCID 14798—
ReactantPotassium NitrateHCID 24434—
SolventSulfuric AcidHCID 1118—
SolventEthyl AcetateHCID 8857—
ProductBenzenamine, 4-methoxy-3-nitro-HCID 12307177%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

To a stirred solution of 30.0 g (244 mmol) p-anisidine in 105 ml concentrated sulfuric acid at 0° C. was added 17.6 g (292 mmol) urea. After stirring for 1 h, a solution of 27.1 g (268 mmol) potassium nitrate in 47 ml concentrated sulfuric acid was then added dropwise over 1 h while the reaction mixture was maintained at 5-10° C. The mixture was then poured onto ice, and sodium hydroxide pellets added portionwise with stirring until the pH was 14. Ethyl acetate was then added and the phases were separated. The organic phase was washed with water and then with brine, dried over sodium sulfate, and concentrated in vacuo to afford 31.4 g (77%) 4-methoxy-3-nitro-phenylamine as an orange solid. EI-MS m/e (%): 169 (M+, 100), 153 ([M-CH3]+, 10), 92 (21).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713499B2
Source datasetuspto-grants-2004_03
ORD IDord-c3efeb78626247de87e868c249c3882b
Source noteuspto-grants-2004_03