戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 894925作成日:2026年10月26日

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

https://huagongshe.com/reaction/894925

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotolueneHCID 8462—
反応物Sodium MethoxideHCID 10942334—
反応物2-Amino-6-fluoro-4-trifluoromethylphenolHCID 13013673—
生成物2-Nitro-4-trifluoromethylanisoleHCID 96748—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04285723
出典データセットuspto-grants-1981_08
ORD IDord-f2a9138a863c4f1d8d80ba02c64ff258
出典メモuspto-grants-1981_08