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HRID 1267314Erstellt: 25. Oktober 2026

Hydrochloric Acid → 5-Iodo-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine

https://huagongshe.com/reaction/1267314

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium IodideHCID 4875—
Edukt5-Amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridineHCID 11087722—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
Produkt5-Iodo-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridineHCID 18546168119,9%

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

To a mixture of 5amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine (10.0 g), conc. HCl (8.47 ml) and acetone (100 ml) was added dropwise a solution of sodium nitrite (NaNO2) (2.46 g) in water (10 ml) at temperatures below 10° C. The mixture was stirred for 30 minutes at 10° C., to which was dropwise added a solution of potassium iodide (KI) (2.46 g) in water (10 ml) at 10° C. The reaction mixture was stirred for further one hour at temperatures raging from 30 to 35° C. and for another one hour at temperatures ranging from 35 to 40° C., followed by concentration under reduced pressure. The concentrate was poured into water, which was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), then the solvent was distilled off under reduced pressure. The residual oily product was subjected to a silica gel chromatography. From the fractions eluted with ethyl acetate-hexane (1:3, v/v) was obtained 5-iodo-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine (7.22 g, 52%). Recrystallization from ethyl acetate-hexane gave colorless crystals, m.p.105-106° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06552058B1
Quelldatensatzuspto-grants-2003_04
ORD IDord-f991b5d1cd8b47f4b1510e0211ced65c
Quellennotizuspto-grants-2003_04