참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene | HCID 8462 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 2-Amino-6-fluoro-4-trifluoromethylphenol | HCID 13013673 | — |
| 생성물 | 2-Nitro-4-trifluoromethylanisole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04285723 |
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| 출처 데이터셋 | uspto-grants-1981_08 |
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| ORD ID | ord-f2a9138a863c4f1d8d80ba02c64ff258 |
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| 출처 메모 | uspto-grants-1981_08 |
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