Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 583005Erstellt: 26. Oktober 2026

Hexadecane → N-(methoxycarbonyl)-4-keto-D-proline methyl ester

https://huagongshe.com/reaction/583005

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexadecaneHCID 11006—
EduktN-(methoxycarbonyl)-4-keto-L-proline methyl esterHCID 53913858—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelSodium AcetateHCID 517045—
ProduktN-(methoxycarbonyl)-4-keto-D-proline methyl esterHCID 11275680—

Reaktionsschritte

An aqueous solution (5.0 mL) containing 25 mM N-(methoxycarbonyl)-4-keto-Dproline methyl ester and 25 mM N-(methoxycarbonyl)-4-keto-L-proline methyl ester in 0.200M sodium acetate (pH 5.0) was mixed with 2.5 g of immobilized Candida antartica lipase fraction B (Boehringer Mannheim, CHIRAZYME® L-2, c.-f., C2, lyo.) at 25° C. The reaction mixture was analyzed after 31 h by mixing the entire reaction mixture with 5.0 mL of 20 mM hexadecane in dichloromethane for 10 minutes, which resulted in the complete extraction of the unreacted D- and L-isomers. The dichloromethane extract was then analyzed by chiral gas chromatography on a Chiraldex G-TA column (Advanced Separation Technologies, Inc., 50 m×0.32 mm ID) to determine the amounts of the unreacted D- and L-isomers. After 31 h, an 85% enantiomeric excess of N-(methoxycarbonyl)-4-keto-D-proline methyl ester was obtained at 41% conversion of the racemic mixture.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05928933
Quelldatensatzuspto-grants-1999_07
ORD IDord-b4e20b41f8c94ccfb563ade87bed2390
Quellennotizuspto-grants-1999_07