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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910745Generated: October 26, 2026

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

https://huagongshe.com/reaction/1910745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantAmmonium formateHCID 2723923—
SolventFormic AcidHCID 284—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product4-Phenyl-1,3-oxazoleHCID 58927934.3%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604029B2
Source datasetuspto-grants-2013_12
ORD IDord-3453bd071969401f831ba76e5a9d13af
Source noteuspto-grants-2013_12