HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 894925Erstellt: 24. Oktober 2026
4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene → 2-Nitro-4-trifluoromethylanisole
https://huagongshe.com/de/reaction/894925
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene | HCID 8462 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | HCID 13013673 | HCID 13013673 | — |
| Produkt | 2-Nitro-4-trifluoromethylanisole | HCID 96748 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04285723 |
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| Quelldatensatz | uspto-grants-1981_08 |
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| ORD ID | ord-f2a9138a863c4f1d8d80ba02c64ff258 |
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| Quellennotiz | uspto-grants-1981_08 |
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