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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160836Generated: October 25, 2026

Water → 2,6-Dimethyl-4-[3-(methylamino)-4-nitrophenoxy]aniline

https://huagongshe.com/reaction/1160836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Amino-3,5-dimethylphenolHCID 76543—
Reactant5-chloro-N-methyl-2-nitroanilineHCID 258041—
ReactantPotassium tert-butoxideHCID 23665647—
Catalyst2,6-Di-tert-butyl-4-methylphenolHCID 31404—
SolventDimethylacetamideHCID 31374—
Product2,6-Dimethyl-4-[3-(methylamino)-4-nitrophenoxy]anilineHCID 6670166593%

Reaction Steps

To a solution of N-(5-chloro-2-nitrophenyl)-N-methylamine (8.00 g) in N,N-dimethylacetamide (112 ml) was added 2,6-di-t-butyl-4-methylphenol (0.24 g). Furthermore, to the resulting mixture were added 4-amino-3,5-dimethylphenol (6.47 g) and potassium t-butoxide (5.29 g) with stirring, and the resulting mixture was stirred at 60° C. for 30 minutes. After stirring, water (4 ml) was added to the reaction mixture, and furthermore water (120 ml) was added dropwise over a 2-hour interval, and then the resulting mixture was cooled gradually to room temperature. The crystalline solid precipitated was collected by filtration, washed with water (80 ml) and dried in vacuo to afford the title compound (11.45 g, yield: 93%) as a yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816552B2
Source datasetuspto-grants-2010_10
ORD IDord-7af7d881506b4340ae6ccfe9b571051e
Source noteuspto-grants-2010_10