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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 491631Erstellt: 26. Oktober 2026

4-Chloro-2-nitroaniline → 3-(4-amino-3-nitro-phenoxy)-N-methyl-benzamide

https://huagongshe.com/reaction/491631

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Chloro-2-nitroanilineHCID 6979—
EduktSodium hydrideHCID 24758—
Edukt3-hydroxy-N-methylbenzamideHCID 353710—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(4-amino-3-nitro-phenoxy)-N-methyl-benzamideHCID 69017532—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 3-hydroxy-N-methyl-benzamide (Step A, 700 mg, 4.6 mmol, 1.0 eq.) in anhydrous DMF (10 mL) was added NaH (200 mg, 5.1 mmol, 1.1 eq.). The reaction was stirred for 10 min. at RT after which 4-chloro-2-nitro-phenylamine (2.0 g, 11.6 mmol, 2.5 eq.) was added. The resulting mixture was heated to 80° C. for 4 h. The reaction was quenched with NaHCO3 (aq.), diluted with CH2Cl2 (50 mL), and washed with 1 N NaOH (25 mL). The organic layer was dried over MgSO4, filtered and concentrated. The crude was further purified by column chromatography (0-100% EtOAc in hexanes) to give pure 3-(4-amino-3-nitro-phenoxy)-N-methyl-benzamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07531553B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-d9c24b3c6a0d486cb91bee5fb968016a
Quellennotizuspto-grants-2009_05