Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 459779Erstellt: 25. Oktober 2026

Ammonium Chloride → 3-(3-amino-4-methoxybenzylidene)-3H-isobenzofuran-1-one

https://huagongshe.com/reaction/459779

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt3-(4-methoxy-3-nitrobenzylidene)-3H-isobenzofuran-1-oneHCID 68624699—
KatalysatorIronHCID 23925—
LösungsmittelWaterHCID 962—
Produkt3-(3-amino-4-methoxybenzylidene)-3H-isobenzofuran-1-oneHCID 6862488965,6%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A stirred mixture of the above crude 3-(4-methoxy-3-nitrobenzylidene)-3H-isobenzofuran-1-one (2.5 g, 0.0085 mol), industrial methylated spirit (40 ml), water (30 ml) and ammonium chloride (0.91 g, 0.017 mol) was heated to 70° C., and iron powder (4.76 g, 0.085 gatom) was added in portions. When the addition was complete, the stirred mixture was heated under reflux for a further 2 hours, then it was filtered while hot through Celite. The collected inorganic solids were washed with hot industrial methylated spirit (3×80 ml), then the filtrate and washings were combined and the solvent was removed in vacuo. The residue was triturated with water (50 ml) and the resulting solid was collected by filtration and dissolved in ethyl acetate (300 ml). The solution was filtered, the filtrate was concentrated in vacuo and the residue was triturated with industrial methylated spirit (10 ml). The resulting solid was collected by filtration and dried in vacuo for 24 hours to give 3-(3-amino-4-methoxybenzylidene)-3H-isobenzofuran-1-one (1.49 g) as a yellow solid, m.pt. 148–153° C.; m/z (M+H)+. 268, 100% purity.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196085B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-0419308258f84f33aab2a1ca61857766
Quellennotizuspto-grants-2007_03