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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222848Generated: October 30, 2026

P-Anisidine → N-(4-Methoxyphenyl)-2-nitroaniline

https://huagongshe.com/reaction/222848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
SolventEthyl AcetateHCID 8857—
ProductN-(4-Methoxyphenyl)-2-nitroanilineHCID 61850499%

Reaction Conditions

Temperature110 °C

Reaction Steps

To 3.7 mL of 2-fluoro-nitrobenzene are added 8.73 g of 4-methoxyaniline (2 equivalents). The whole is heated to 110° C. overnight. The medium is taken up in ethyl acetate, successively washed with water, a saturated solution of sodium bicarbonate and then with a saturated solution of sodium chloride. The organic phase is dried on magnesium sulfate, filtered and then concentrated under reduced pressure. With silica gel chromatography of the residue (petroleum ether/ethyl acetate: 90/10) 8.63 g of the desired product are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207373B2
Source datasetuspto-grants-2012_06
ORD IDord-06e9bd1f1a3345fc94d11acd078d8eba
Source noteuspto-grants-2012_06