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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28583생성일: 2026년 10월 24일

5-(4-Nitrophenyl)-1,3-oxazole → 4-(1,3-Oxazol-5-yl)aniline

https://huagongshe.com/ko/reaction/28583

반응식

참여 물질

역할이름HCID투입량
반응물5-(4-Nitrophenyl)-1,3-oxazoleHCID 2737068—
촉매IronHCID 23925—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물4-(1,3-Oxazol-5-yl)anilineHCID 51774783.2%

반응 조건

온도60 °C

반응 단계

A mixture of 5-(4-nitro-phenyl)-oxazole (2.0 g, 10.5 mmol), iron powder (2.4 g, 42.8 mmol) in acetic acid (5 ml) and methanol (30 ml) was stirred at 60° C. for 1 hour. After filtration through a pad of celite under suction, the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography eluting with ethyl acetate-hexane (3:4 followed by 3:2) to give 4-oxazol-5-yl-phenyl-amine (1.4 g, 83% yield). 1H NMR (acetone-d6) δ 5.0 (br s, 2H, NH), 6.76 (d, 2H, J=8.7 Hz, Ar), 7.12 (s, 1H, Ar), 7.45 (d, 2H, J=8.6 Hz, Ar), 8.04 (s, 1H, Ar).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419984B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-6f1e12607b364e42a2848d5e70461bf3
출처 메모uspto-grants-2008_09