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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1194370Erstellt: 26. Oktober 2026

1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → alpha-(4H-1,3-Benzodioxin-6-yl)-1-triphenylmethyl-1H-imidazole-4-methanol

https://huagongshe.com/reaction/1194370

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
Edukt6-Bromo-4H-1,3-benzodioxineHCID 14520337—
Produktalpha-(4H-1,3-Benzodioxin-6-yl)-1-triphenylmethyl-1H-imidazole-4-methanolHCID 1452034453%

Reaktionsschritte

This compound is prepared like the preceding compound but starting from 6-bromo-4H-1,3-benzodioxin and 1-triphenylmethyl-1H-imidazole-4-carboxaldehyde. After decomposing the reaction mixture, the reaction product is extracted with dichloromethane and recrystallized from isopropyl alcohol. By chromatography of the residue obtained after evaporation of the mother liquors, there is obtained a second crop of product. Yield: 53% of theory; M.P.: 165°-167° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04814343
Quelldatensatzuspto-grants-1989_03
ORD IDord-8522ab1a0ab442ca861b3c58720b5f57
Quellennotizuspto-grants-1989_03