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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1375142Erstellt: 24. Oktober 2026

Ethanol → alpha-(Aminomethyl)-4-methoxybenzyl alcohol

https://huagongshe.com/de/reaction/1375142

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktHydroxylamineHCID 787—
Edukt4-MethoxybenzaldehydeHCID 31244—
EduktFumaric AcidHCID 444972—
EduktAluminium lithium hydrideHCID 21226445—
Produktalpha-(Aminomethyl)-4-methoxybenzyl alcoholHCID 3016949—

Reaktionsschritte

2-Amino-1-(4-methoxyphenyl)ethanol was prepared according to the procedure of Evans et al., J. Org. Chem., 39, 914 (1974) by cyanosilylation of 4-methoxybenzaldehyde followed by lithium aluminum hydride reduction. The crude aminoalcohol (36.9 g) was dissolved in 150 mL of hot ethanol on a steam bath. To this mixture was slowly added 12.83 g of fumaric acid. The precipitated salt was filtered and washed with additional ethanol. Recrystallization from methanol provided greater than 99% pure 2:1 amine:fumarate salt.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07166696B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-d5b66ae479b541ba8a29b81f52689dbd
Quellennotizuspto-grants-2007_01