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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14499Erstellt: 23. Oktober 2026

Acetic Acid → 3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-4-oxo-4H-chromene-8-carbaldehyde

https://huagongshe.com/de/reaction/14499

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
EduktHexamethylenetetramineHCID 4101—
Edukt3-(4-Chlorophenyl)-7-hydroxy-2-isopropyl-chromen-4-oneHCID 16202451—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-4-oxo-4H-chromene-8-carbaldehydeHCID 86625608—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-chromen-4-one (12.48 g, 39.6 mmol) and hexamethylenetetramine (39.46 g, 0.28 mol) in acetic acid (250 ml) is stirred at 100° C. for 20 h. After the mixture has cooled to room temperature, the solvent is removed in vacuo to afford a black oily residue. 5M HCl solution (150 ml) is added, and the mixture is heated under reflux for 30 min. The reaction mixture is poured onto ice/water, and the resulting brown solid is isolated by filtration. The solid is taken up in dichloromethane, the mixture is passed through a bed of Celite, and the solvent is evaporated in vacuo. The solid residue is stirred at room temperature with ethyl acetate, filtered and washed with hexane to afford the desired product as a pale brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732435B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-e03fad2a09ea4f109a4d38cc1e388195
Quellennotizuspto-grants-2010_06