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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1910745Erstellt: 26. Oktober 2026

Phenacyl bromide → 4-Phenyl-1,3-oxazole

https://huagongshe.com/reaction/1910745

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenacyl bromideHCID 6259—
EduktAmmonium formateHCID 2723923—
LösungsmittelFormic AcidHCID 284—
LösungsmittelWaterHCID 962—
LösungsmittelSodium HydroxideHCID 14798—
Produkt4-Phenyl-1,3-oxazoleHCID 58927934,3%

Reaktionsschritte

A solution of phenacyl bromide (4 g, 20.1 mmol) and ammonium formate (4.4 g, 70.35 mmol) in formic acid (20 mL) was refluxed for 5 h. The deep red mixture was cooled to r.t., diluted with water and basified with dilute sodium hydroxide solution. This was extracted with ethyl acetate (×3), then the combined organic layers were washed with water and brine, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (60-120 mesh), eluting with 20% ethyl acetate-petroleum ether, to afford 4-phenyloxazole (1 g, 34%) as a pale yellow oil which solidifies at −20° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08604029B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-3453bd071969401f831ba76e5a9d13af
Quellennotizuspto-grants-2013_12