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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1089657Erstellt: 24. Oktober 2026

DL-Ephedrine → Pseudoephedrine

https://huagongshe.com/de/reaction/1089657

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDL-EphedrineHCID 5032—
EduktMethylamineHCID 6329—
EduktEphedrineHCID 9294—
ProduktPseudoephedrineHCID 7028—

Reaktionsschritte

The combination of yeast transformation of benzaldehyde to produce PAC and chemical conversion of the PAC to make 1-ephedrine is described in U.S. Pat. No. 1,956,950. The PAC can be converted by a chemical reductive amination with methylamine to optically pure L-ephedrine as follows: ##STR2## The 1-ephedrine can then converted in high yield to d-pseudoephedrine as follows: ##STR3## It is apparent from this reaction scheme that microbial transformation of benzaldehyde by yeast to form L-(-)phenyl acetyl carbinol in high yield and purity is of prime importance for successful commercial operation of the synthetic route.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05079145
Quelldatensatzuspto-grants-1992_01
ORD IDord-c9ee2c214413439988f36bc372be76e0
Quellennotizuspto-grants-1992_01