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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14486Erstellt: 24. Oktober 2026

Water → 3-Bromo-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-one

https://huagongshe.com/de/reaction/14486

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-MethoxybenzylamineHCID 75452—
Edukt2,4,6-trimethyl-benzenesulfonic acid 3-bromo-2-isopropyl-8-nitro-4-oxo-4H-chromen-7-yl esterHCID 86625615—
LösungsmittelTolueneHCID 1140—
Produkt3-Bromo-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-oneHCID 68703155—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

To a solution of 2,4,6-trimethyl-benzenesulfonic acid 3-bromo-2-isopropyl-8-nitro-4-oxo-4H-chromen-7-yl ester (1.906 g, 3.5 mmol) in dry toluene (18 ml) in a 20 ml capacity microwave tube is added p-methoxybenzylamine (0.69 ml, 5.26 mmol). The mixture is heated at 130° C. under microwave irradiation for 90 minutes and then at 140° C. under microwave irradiation for a further 30 minutes. Water (40 ml) is added, and the mixture is extracted with ethyl acetate (3×100 ml). The ethyl acetate extracts are combined, washed with saturated brine (50 ml), dried (MgSO4), filtered and evaporated. The crude product is purified by chromatography on silica gel using cyclohexane-ethyl acetate (8:1) as eluant. The product-containing fractions are evaporated under reduced pressure, and the residue is triturated with diethyl ether to give a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732435B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-24bdd29273584eb289dff4c68aa8064e
Quellennotizuspto-grants-2010_06