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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 74157Erstellt: 23. Oktober 2026

Hydrochloric Acid → 4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acid

https://huagongshe.com/de/reaction/74157

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
Edukt4-Fluoro-3-nitrobenzoic acidHCID 67987—
Edukt4-AminotetrahydropyranHCID 419223—
EduktOxan-2-amineHCID 14471248—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acidHCID 43610332101,2%

Reaktionsschritte

4-Fluoro-3-nitrobenzoic acid (126.4 g, 0.68 mol) was dissolved in ethanol (880 mL). Triethylamine (82.6 g, 0.82 mol), 4-aminotetrahydropyran (82.7 g, 0.81 mol) were added in turn dropwise, and after the additions the reaction solution was heated to reflux. After refluxing for 5 h, triethylamine (8.3 g, 82 mmol), aminotetrahydropyran (8.3 g, 81 mmol) were added, and this was refluxed for a further 9 hours. After the reaction mixture was allowed to cool to room temperature, 2N HCl (880 mL) and water (880 mL) were added and after stirring for awhile, the solid obtained was filtered off. This was forced air-dried at 60° C. to yield the title compound (183.3 g, quant.) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829035B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-3d585bfc7faf417584411f9094ad5215
Quellennotizuspto-grants-2014_09