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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 459755Erstellt: 24. Oktober 2026

Triethylamine → 3-(4-fluoro-3-nitrobenzylidene)-3H-isobenzofuran-1-one

https://huagongshe.com/de/reaction/459755

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-Fluoro-3-nitrobenzaldehydeHCID 598129—
EduktDimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonateHCID 11118213—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(4-fluoro-3-nitrobenzylidene)-3H-isobenzofuran-1-oneHCID 68624589—

Reaktionsschritte

A stirred solution of dimethyl 3-oxo-1,3-dihydroisobenzofuran-1-ylphosphonate (20 g, 0.083 mol) and 4-fluoro-3-nitrobenzaldehyde (13.97 g, 0.083 mol) in tetrahydrofuran (120 ml) was cooled to 15° C. and triethylamine (11.5 ml, 0.083 mol) was added dropwise at <25° C. The mixture thickened at this point, so further tetrahydrofuran (50 ml) was added to aid stirring. The mixture was stirred at ambient temperature for 65 hours and the resulting solid was collected by filtration. The filtrate was concentrated in vacuo, the residue was triturated with water (30 ml) and the resulting solid was collected by filtration. The two crops of solid were combined and suspended in water (120 ml). The mixture was stirred at ambient temperature for 30 minutes and the resulting solid was collected by filtration and dried in vacuo for 24 hours to give crude 3-(4-fluoro-3-nitrobenzylidene)-3H-isobenzofuran-1-one, still slightly wet with water, which was used directly in the next stage.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196085B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-3b69a254da05497aae7b0e857a4bf4d4
Quellennotizuspto-grants-2007_03