HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1428997Erstellt: 25. Oktober 2026
Triethylamine → 2-Fluoro-4-(trifluoromethyl)aniline
https://huagongshe.com/reaction/1428997
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Edukt | 2-Fluoro-4-(trifluoromethyl)benzoic acid | HCID 518003 | — |
| Katalysator | Cuprous chloride | HCID 62652 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | 2-Fluoro-4-(trifluoromethyl)aniline | HCID 2737674 | 58% |
Reaktionsschritte
To the solution of 2-fluoro-4-(trifluoromethyl)benzoic acid (1 kg, 4.805 mol, 1.00 equivalent “eq.”) and CuCl (14.26 g, 0.144 mol, 0.03 eq.) in t-BuOH (11.7 L) was added triethylamine (TEA, 533.8 g, 5.286 mol, 1.10 eq.) dropwise at room temperature (rt). Then the solution was heated to 50° C. and diphenylphosphoryl azide (DPPA, 1393 g, 5.045 mol, 1.05 eq.) was added dropwise to the solution at 50-60° C. After heating at 80-85° C. overnight the solution was concentrated under vacuum. The residual was dissolved in H2O and filtered. The filtrate was extracted with ethyl acetate. The organic layers was dried with Na2SO4, filtered and concentrated under vacuum. The residual was dissolved in tent-Butyl methyl ether (TBME) and HCl (gas) was bubbled in for 2 hours. The filtrate was collected and dissolved in water and basified with 2 M NaOH. The solution was extracted with TBME. The organic layers were dried and concentrated under vacuum to give 2-fluoro-4-(trifluoromethyl)aniline (498 g, 58%) as a red oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08937185B2 |
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| Quelldatensatz | uspto-grants-2015_01 |
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| ORD ID | ord-7e9b73f7c53c4a14a8f70a7579039688 |
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| Quellennotiz | uspto-grants-2015_01 |
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