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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36616Erstellt: 24. Oktober 2026

Formaldehyde → 2,2-Dimethyl-6-(1H-imidazol-1-YL)benzopyran

https://huagongshe.com/de/reaction/36616

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktGlyoxalHCID 7860—
EduktAmmonium HydroxideHCID 14923—
EduktAmmonium AcetateHCID 517165—
Edukt2,2-Dimethyl-2H-chromen-6-amineHCID 10080881—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
Produkt2,2-Dimethyl-6-(1H-imidazol-1-YL)benzopyranHCID 19937600—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a stirred solution of 20 g (0.11 mol) of 6-amino-2,2-dimethylbenzopyran and 70 g (0.91 mol) of ammonium acetate in 190 mL of acetic acid and 770 mL of MeOH at 65° C. is added dropwise over 0.5 h, a mixture of 11.1 g (0.14 mol) of formaldehyde and 20g (0.14 mol) of glyoxal. The mixture is stirred for 1 hour at 65° C., then poured onto 800 g of ice. The pH of the solution is adjusted to 10 by the addition of concentrated ammonium hydroxide. The mixture is extracted with dichloromethane (3×200 mL) and the combined organic extracts are dried with sodium sulfate, filtered and evaporated under reduced pressure. The resulting oil is subjected to chromatography on silica gel utilizing 3% methanol in dichloromethane as eluent. The eluates are analyzed utilizing thin layer chromatography and appropriate fractions are combined and evaporated to produce the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05416097
Quelldatensatzuspto-grants-1995_05
ORD IDord-90b75e363fa247b8ab5b0c4afb592cd3
Quellennotizuspto-grants-1995_05