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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1048987Erstellt: 26. Oktober 2026

Methyl iodide → 4-Methoxy-N-methyl-2-nitrobenzenamine

https://huagongshe.com/reaction/1048987

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt4-Methoxy-2-nitroanilineHCID 66793—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Methoxy-N-methyl-2-nitrobenzenamineHCID 3554313—

Reaktionsschritte

To a solution of 4-methoxy-2-nitro-phenylamine (5.0 g, 0.029 mol) in DMF (25 ml) was added NaH (0.9 g, 0.035 mol) at 0° C. and stirred at that temperature for 30 min. Methyl iodide (2.17 ml, 0.035 mol) was added and the resulting solution was stirred at room temperature for 30 min. The reaction was quenched with ice-water and extracted with ethyl acetate (3×100 ml). The combined organic layers were washed with brine dried over Na2SO4 and concentrated under vacuum to afford the title compound (4-methoxy-2-nitro-phenyl)-methyl-amine as a red solid. C8H10N2O3; 1H NMR (400 MHz, CDCl3), δ: 8.00 (brs, 1H), 7.62 (d, J=2.4 Hz, 1H), 7.18 (dd,1=9.2 Hz, J2=2.0 Hz, 1H), 6.82 (d, J=9.6 Hz, 1H), 3.81 (d, J=14.8 Hz, 3H), 3.02 (s, 3H). MS (M+1): 183.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09382226B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-6b9c3a64e1ca465fad46e2963325afa1
Quellennotizuspto-grants-2016_07