Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3777Erstellt: 23. Oktober 2026

Boron trifluoride etherate → N-p-Methoxybenzyloxycarbonyl-O-methyl-D-serine benzyl ester

https://huagongshe.com/de/reaction/3777

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron trifluoride etherateHCID 8000—
EduktDiazomethaneHCID 9550—
EduktN-p-methoxybenzyloxycarbonyl-D-serine benzyl esterHCID 13652495—
EduktAcetone cardiceHCID 18522661—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-p-Methoxybenzyloxycarbonyl-O-methyl-D-serine benzyl esterHCID 1365249770%

Reaktionsschritte

The N-p-methoxybenzyloxycarbonyl-D-serine benzyl ester (720 mg, 2.00 mmol) is dissolved in dry dichloromethane (20 ml) and the solution cooled to dry ice/acetone. Boron trifluoride etherate (100 μl) is added followed by the portionwise addition of diazomethane (30 mmol in 20 ml CH2Cl2). After about 30 minutes the solution is filtered and washed once with water (10 ml), then dried (MgSO4) and evaporated to dryness. The resulting residue is chromatographed on silica gel using chloroform as eluant to give the pure title compound as an oil (520 mg, 70%) which crystallises on standing to give a colourless solid of m.p. 68°-69° C.; [α]D20 -1.3° (c 4.0, CHCl3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04722924
Quelldatensatzuspto-grants-1988_02
ORD IDord-3d9fe4eea0d14c78998610d953418f18
Quellennotizuspto-grants-1988_02