Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263455Generated: October 31, 2026

Hydrochloric Acid → 3-Methyl-4-methoxybenzenamine

https://huagongshe.com/reaction/1263455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant1-Methoxy-2-methyl-4-nitrobenzeneHCID 643520—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product3-Methyl-4-methoxybenzenamineHCID 67297123%

Reaction Steps

To a solution of 3-methyl-4-methoxynitrobenzene(7.59 g, 45 mmol) in ethanol was added iron powder (35 g), water(5 mL) and concentrated hydrochloric acid (0.4 mL). The mixture was refluxed for 1 hour and then filtered while hot. The filtrate was concentrated to dryness. The residue was dissolved in chloroform. The chloroform solution was dried with sodium sulfated and evaporated to give 3-methyl-4-methoxyaniline (7.59 g). To a solution of this compound (6.17 g, 45 mmol) in acetic acid (55 mL) were added dropwise acetic anhydride (4,4 mL, 46 mmol) at room temperature with stirring and then bromine(2,4 mL, 46 mmol) at 50° C. with stirring. The reaction mixture was stirred at the same temperature for 2 hours and poured into ice-water. The resulting precipitate was filtered off, washed with water and dissolved in ethyl acetate. This solution was washed with saturated sodium chloride solution, dried with sodium sulfate and evaporated to dryness to give 2-bromo-4-methoxy-5-methylacetanilide as a crude product. Crystallization from diethyl ether gave pure product (8.27 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541470B1
Source datasetuspto-grants-2003_04
ORD IDord-019a305255454f67a35f69caf47269df
Source noteuspto-grants-2003_04