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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1910745생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1910745

반응식

참여 물질

역할이름HCID투입량
반응물Phenacyl bromideHCID 6259—
반응물Ammonium formateHCID 2723923—
용매Formic AcidHCID 284—
용매WaterHCID 962—
용매Sodium HydroxideHCID 14798—
생성물4-Phenyl-1,3-oxazoleHCID 58927934.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08604029B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-3453bd071969401f831ba76e5a9d13af
출처 메모uspto-grants-2013_12