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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 894925생성일: 2026년 10월 25일

4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene → 2-Nitro-4-trifluoromethylanisole

https://huagongshe.com/reaction/894925

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotolueneHCID 8462—
반응물Sodium MethoxideHCID 10942334—
반응물2-Amino-6-fluoro-4-trifluoromethylphenolHCID 13013673—
생성물2-Nitro-4-trifluoromethylanisoleHCID 96748—

반응 단계

The 2-amino-4-trifluoromethylphenols (XI) required for the reaction sequence just described may be prepared by conventional methods. Thus, 2-amino-6-fluoro-4-trifluoromethylphenol may be prepared from 2-nitro-4-trifluoromethylchlorobenzene by reacting the latter with sodium methoxide to give 2-nitro-4-trifluoromethylanisole, and reducing this compound to 2-amino-4-trifluoromethylanisole. The latter compound may be diazotised and converted to its fluoborate salt and heated to give 2-fluoro-4-trifluoromethylanisole. This may then be nitrated to form 2-fluoro-6-nitro-4-trifluoromethylanisole, which is then reduced to give 2-amino-6-fluoro-4-trifluoromethylanisole. Finally the latter compound is heated with a demethylating agent, for example an excess of pyridine hydrochloride to give 2-amino-6-fluoro-4-trifluoromethylphenol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04285723
출처 데이터셋uspto-grants-1981_08
ORD IDord-f2a9138a863c4f1d8d80ba02c64ff258
출처 메모uspto-grants-1981_08