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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1048Erstellt: 23. Oktober 2026

Dimethylformamide → 5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl]-1H-tetrazole

https://huagongshe.com/de/reaction/1048

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktAmmonium ChlorideHCID 25517—
EduktSodium AzideHCID 33557—
Edukt2-(2-Cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuranHCID 10155313—
LösungsmittelWaterHCID 962—
Produkt5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl]-1H-tetrazoleHCID 17841845178,1%

Reaktionsschritte

A mixture of 2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran (1.20 g), sodium azide (1.09 g), ammonium chloride (0.90 g) and N,N-dimethylformamide (30 ml) was stirred at 130° to 140° C. for 16 hours. The reaction mixture was poured over water and extracted with ethyl acetate. After the ethyl acetate layer was washed with water and dried (MgSO4), the solvent was distilled off; the residue was subjected to silica gel column chromatography. From the fraction eluted with methanol-chloroform (5:95, v/v), 5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl ]-1H-tetrazole (1.05 g, 78%) was obtained, which was then recrystallized from dichloromethane-methanol to yield colorless prisms having a melting point of 177° to 178° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723479
Quelldatensatzuspto-grants-1998_03
ORD IDord-2e59b47848294fe195989e641f0b30fb
Quellennotizuspto-grants-1998_03