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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31408Erstellt: 23. Oktober 2026

Methanol → 5-(4-Iodophenyl)-3-methyl-1,2,4-oxadiazole

https://huagongshe.com/de/reaction/31408

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt4-Iodobenzoic acidHCID 12085—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktSodium MethoxideHCID 10942334—
EduktHCID 178465666HCID 178465666—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-(4-Iodophenyl)-3-methyl-1,2,4-oxadiazoleHCID 1970311626%

Reaktionsschritte

1,1′-Carbonyldiimidazole (0.49 g, 3 mmol) was added to a solution of 4-iodobenzoic acid (0.5 g, 2 mmol) in dry dimethylformamide (4 ml) and stirred at room temperature for 30 minutes. N-hydroxy-acetamidine (0.224 g, 3 mmol) was added and stirring at room temperature continued for 16 hours. Sodium methoxide in methanol (25% wt solution; 1.1 ml, 5 mmol) was added and the mixture heated at 80° C. for 6 hours. Once cool, ethyl acetate (50 ml) and water (50 ml) were added. The organic layer was washed with water (50 ml), brine (50 ml), dried over magnesium sulfate, filtered and solvent removed in vacuo. The residue was purified by silica SPE cartridge (5 g) (100% cyclohexane, 20:1 cyclohexane/ethyl acetate v:v to 10:1 cyclohexane/ethyl acetate v:v) to yield the desired product as a white solid (0.15 g, 0.52 mmol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425555B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-2dc827775f15424f9227b48bef98f4d9
Quellennotizuspto-grants-2008_09