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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395758Erstellt: 26. Oktober 2026

Sodium borohydride → 3-Benzyloxy-4-methyl-phenylamine

https://huagongshe.com/reaction/395758

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt2-Benzyloxy-1-methyl-4-nitro-benzeneHCID 18174502—
KatalysatorNickel acetate tetrahydrateHCID 62601—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Benzyloxy-4-methyl-phenylamineHCID 279462597%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of 3-benzyloxy-4-methylnitrobenzene (1.1 g, 4.4 mmol) in tetrahydrofuran (25 mL) and methanol (50 mL) was added nickel acetate tetrahydrate (2.2 g, 8.7 mmol). The solution was cooled to 0° C. and sodium borohydride (0.66 g, 17.4 mmol) was added in small portions. After gas evolution had ceased, the solvents were removed in vacuo and the residue was partitioned between ethyl acetate and concentrated ammonium hydroxide. The layers were separated and the organic phase was washed with ammonium hydroxide followed by saturated aqueous sodium chloride solution, dried (magnesium sulfate), filtered, and concentrated In vacuo to give 0.9 g (97%) of the title product as an off-white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605626B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-45acb0023692450f80e5692efd70658b
Quellennotizuspto-grants-2003_08