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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275866Erstellt: 26. Oktober 2026

Acetic Acid → 2-[2-(4-Benzyloxyphenyl)ethyl]amino-alpha-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcohol

https://huagongshe.com/reaction/275866

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt4-BenzyloxyphenylacetaldehydeHCID 11413489—
Edukt2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 54358865—
EduktHCID 178511852HCID 178511852—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-[2-(4-Benzyloxyphenyl)ethyl]amino-alpha-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcoholHCID 54258279—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

In methanol (15 ml) were dissolved 2-amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol produced in Example 1-(2) (0.5 g) and 4-benzyloxyphenylacetaldehyde (0.4 g). To the solution were added acetic acid (0.1 g) and, subsequently, cyano sodium hydride (0.11 g). The mixture was stirred for 40 minutes at 60° C. The reaction mixture was diluted with ethyl acetate (60 ml), which was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to leave 2-[2-(4-benzyloxyphenyl)ethyl]amino-α-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcohol (0.45 g) as a colorless oily product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352982B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-1c8c5b7df28743a49d051f48e5d4a748
Quellennotizuspto-grants-2002_03