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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 918129생성일: 2026년 10월 25일

4-Fluoroiodobenzene → 4-Acetyl-4'-fluoro-2-nitrobiphenyl

https://huagongshe.com/reaction/918129

반응식

참여 물질

역할이름HCID투입량
반응물4-FluoroiodobenzeneHCID 9605—
반응물1-(4-Bromo-3-nitrophenyl)ethan-1-oneHCID 87737—
용매MethanolHCID 887—
생성물4-Acetyl-4'-fluoro-2-nitrobiphenylHCID 21320555—

반응 단계

4-fluoroiodobenzene and 4-bromo-3-nitroacetophenone were reacted in an analogous manner to that described in Example 1 (a) to give the novel intermediate 4-acetyl-4'-fluoro-2-nitrobiphenyl, m.p. 88° - 90°C. (from methanol). This compound was reduced with stannous chloride in concentrated hydrochloric acid in an analogous manner to that described in Example 1 (b) to give the novel intermediate 4-acetyl-2-amino-4'-fluorobiphenyl, m.p. 88° - 91°C. (from methanol). The amino group in this compound was converted to methoxy in the following way:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03969402
출처 데이터셋uspto-grants-1976_07
ORD IDord-fffb69d45e50446d86828345be52bdd9
출처 메모uspto-grants-1976_07