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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77721Erstellt: 23. Oktober 2026

Hydrochloric Acid → 5-(Trifluoromethyl)pyridin-3-amine

https://huagongshe.com/de/reaction/77721

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktHydroxylamineHCID 787—
Edukt2-Chloro-3-nitro-5-(trifluoromethyl)pyridineHCID 4736950—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt5-(Trifluoromethyl)pyridin-3-amineHCID 140519368%

Reaktionsschritte

2-Chloro-3-nitro-5-(trifluoromethyl)pyridine (0.850 g, 3.75 mmol) was dissolved in methanol (17 mL) and palladium on carbon (800 mg of 10%, 50% wet, 0.375 mmol) was added. The mixture was hydrogenated at 60 psi and 20° C. for 16 h. LCMS showed no remaining starting material or hydroxylamine (M+H 213/215, 3:1) intermediate, and showed a mixture of partially reduced product (M+H 163; UVmax 214, 258, & 332 nm) and the fully reduced product (M+H 169; no UV). The mixture was filtered; and the filtrate was rinsed thoroughly, and concentrated in vacuo to give 0.74 g, of the product as the HCl salt. The product was purified by prep HPLC/MS using a 30 mm×100 mm C18 column; 20% CH3CN—H2O (0.1% NH4OH), 1 min, to 40% at 6 min; 60 mL/min; detector set at m/z 163; retention time, 4.4 min. Fractions containing the pure product were combined and concentrated to give an oil, 52 mg, 8% yield. 1H NMR (CDCl3) δ 8.26 (s, 1H); 8.24 (d, 1H); 7.15 (t, 1H); 4.00 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841318B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-678054e7bcd244019686071c0783536f
Quellennotizuspto-grants-2014_09