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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1160839Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1160839

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
Edukt2,4-DichloronitrobenzeneHCID 11899—
Edukt4-Amino-3,5-dimethylphenolHCID 76543—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylacetamideHCID 31374—
Produkt2,6-Dimethyl-4-[3-(methylamino)-4-nitrophenoxy]anilineHCID 6670166567%

Reaktionsbedingungen

Temperatur77.5 °C

Reaktionsschritte

To a solution of 2,4-dichloronitrobenzene (3.0 g) in N,N-dimethylacetamide (30 ml) was added a 40% aqueous solution of methylamine (4.9 g) at room temperature, and the resulting mixture was stirred at 75-80° C. for 1.5 hours. To the reaction mixture were added 4-amino-3,5-dimethylphenol (2.2 g), potassium t-butoxide (3.5 g), and N,N-dimethylacetamide (15 ml), and the resulting mixture was stirred at the same temperature for 3 hours. After stirring, water (60 ml) was added to the reaction mixture, and the resulting mixture was cooled gradually to room temperature. The crystalline solid precipitated was collected by filtration and dried in vacuo to afford the title compound (3.0 g, yield: 67%) as a yellow crystalline solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07816552B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-553cb165e6454b8583fe610a05b79e66
Quellennotizuspto-grants-2010_10