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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275878Erstellt: 26. Oktober 2026

Acetic Acid → 2-(3,4-Dibenzyloxybenzyl)amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol

https://huagongshe.com/reaction/275878

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt3,4-Bis(benzyloxy)benzaldehydeHCID 79526—
Edukt2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 54358865—
EduktHCID 178511851HCID 178511851—
LösungsmittelMethanolHCID 887—
Produkt2-(3,4-Dibenzyloxybenzyl)amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 5442387875,5%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

In methanol (20 ml) were dissolved 2-amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.6 g) and 3,4-dibenzyloxybenzaldehyde (0.55 g). To the solution were added acetic acid (0.12 g) and cyano sodium borohydride (0.13 g). The mixture was stirred for 1.5 hour at 60° C. The reaction mixture was concentrated, to which were added water (50 ml) and ethyl acetate (80 ml), followed by extraction. The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to leave 2-(3,4-dibenzyloxybenzyl)amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.83 g) as colorless crystals, m.p.: 118-120° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352982B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-f1156755ca1643af932a9577860a226c
Quellennotizuspto-grants-2002_03