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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 727806Erstellt: 25. Oktober 2026

Water → 4-(Quinolin-2-ylmethoxy)aniline

https://huagongshe.com/reaction/727806

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktHydrazine hydrate (1:1)HCID 24654—
Edukt2-[(4-Nitrophenoxy)methyl]quinolineHCID 13770360—
KatalysatorNickelHCID 935—
LösungsmittelMeOH tetrahydrofuranHCID 21899815—
Produkt4-(Quinolin-2-ylmethoxy)anilineHCID 2747569—

Reaktionsbedingungen

Temperatur35 °C

Reaktionsschritte

117.8 g (0.42 mol) of 2-(4-nitrophenoxymethyl)quinoline were dissolved in 1 l of methanol/tetrahydrofuran (1:1). About 5 g of Raney nickel were then added and the mixture was warmed to 35° C. 63.1 g (1.26 mol) of hydrazine hydrate ×H2O were then added dropwise and the mixture was stirred overnight. The residue was filtered off, the solution was concentrated in vacuo and the residue was taken up with methylene chloride. The mixture was then washed with water and conc. hydrochloric acid was added to the organic phase. The precipitate deposited was filtered off, washed with 2 N hydrochloric acid, dissolved in water and rendered alkaline with 20% strength NaOH. The residue was dried in vacuo.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05045547
Quelldatensatzuspto-grants-1991_09
ORD IDord-ed44bba192c04457973ed487570d6496
Quellennotizuspto-grants-1991_09