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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1160836Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1160836

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-Amino-3,5-dimethylphenolHCID 76543—
Edukt5-chloro-N-methyl-2-nitroanilineHCID 258041—
EduktPotassium tert-butoxideHCID 23665647—
Katalysator2,6-Di-tert-butyl-4-methylphenolHCID 31404—
LösungsmittelDimethylacetamideHCID 31374—
Produkt2,6-Dimethyl-4-[3-(methylamino)-4-nitrophenoxy]anilineHCID 6670166593%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07816552B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-7af7d881506b4340ae6ccfe9b571051e
Quellennotizuspto-grants-2010_10