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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 74186Erstellt: 23. Oktober 2026

Methanol → 5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline

https://huagongshe.com/de/reaction/74186

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)nitrobenzeneHCID 67498108—
KatalysatorPalladiumHCID 23938—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 6749880689,1%

Reaktionsschritte

5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)nitrobenzene (see Working Example 20-1) (1.00 g, 0.76 mol) was dissolved in a solvent mixture of THF (50 mL) and methanol (50 mL), and Pd/C (5%, wet, 0.5 g) was added to carry out a hydrogenation reaction. After being stirred overnight at room temperature, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to yield the title compound (812 mg, 89.1%) as a gray solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829035B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-db448fdc435e4d0a9b8ec2680e8c8fa4
Quellennotizuspto-grants-2014_09