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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1076451생성일: 2026년 10월 26일

Nitric Acid → N-(4-Nitro-2-phenoxyphenyl)acetamide

https://huagongshe.com/reaction/1076451

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물2-Nitrophenyl phenyl etherHCID 16661—
반응물Benzenamine, 2-phenoxy-HCID 75899—
반응물2-PhenoxyacetanilideHCID 897080—
용매Acetic AcidHCID 176—
생성물N-(4-Nitro-2-phenoxyphenyl)acetamideHCID 2153677260%

반응 단계

o-Nitrophenyl phenyl ether was reduced catalytically to o-phenoxyaniline, m. 43°-5°, which was acetylated to 2'-phenoxyacetanilide, m. 82°-4°. Yields from both reactions were essentially quantitative. The 2'-phenoxy-acetanilide was dissolved in acetic acid and treated at 60°-80° with red fuming nitric acid to produce a 60-70% yield of 4'-nitro-2'-phenoxy-acetanilide, m. 176°-183°. This was deacetylated by refluxing with methanolic hydrochloric acid to 4-nitro-2-phenoxyaniline, m. 116°-8°. The yield was 99% of theoretical.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03957489
출처 데이터셋uspto-grants-1976_05
ORD IDord-ce464954457241a680b969b2492d6c21
출처 메모uspto-grants-1976_05