関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene | HCID 8462 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | 2-Amino-6-fluoro-4-trifluoromethylphenol | HCID 13013673 | — |
| 生成物 | 2-Nitro-4-trifluoromethylanisole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04285723 |
|---|
| 出典データセット | uspto-grants-1981_08 |
|---|
| ORD ID | ord-f2a9138a863c4f1d8d80ba02c64ff258 |
|---|
| 出典メモ | uspto-grants-1981_08 |
|---|