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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 919166Erstellt: 25. Oktober 2026

Triethylamine → 2-Fluoro-4-(trifluoromethyl)aniline

https://huagongshe.com/reaction/919166

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Edukt2-Fluoro-4-(trifluoromethyl)benzoic acidHCID 518003—
KatalysatorCuprous chlorideHCID 62652—
Lösungsmitteltert-ButanolHCID 6386—
Produkt2-Fluoro-4-(trifluoromethyl)anilineHCID 273767458%

Reaktionsbedingungen

Temperatur50 °C

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 tert-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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09273007B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-d935a6917e6944fb8540c86ba1aaf421
Quellennotizuspto-grants-2016_03