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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 534678Erstellt: 26. Oktober 2026

Trifluoroacetic acid → N-benzyl-O-benzyl-D-serinamide

https://huagongshe.com/reaction/534678

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktN-benzyl-O-benzyl-N2-Boc-D-serinamideHCID 7216909—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-benzyl-O-benzyl-D-serinamideHCID 6708283370%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To a solution of N-benzyl-O-benzyl-N2-Boc-D-serinamide (3 g) and dichloromethane (15 mL), trifluoroacetic acid (15 mL) was added. The solution was stirred for 2 hours at 40° C. for completion of reaction. The solution was concentrated under vacuum to remove solvents and subsequently water was added. The aqueous layer was basified to pH 8-10 with 5% sodium hydroxide. The aqueous layer was extracted with ethyl acetate and the combined organic layer was washed with brine solution. Organic layer was concentrated under vacuum to obtain an oily residue solidify by n-Hexane to give 1.55 g of N-benzyl-O-benzyl-D-serinamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08853439B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-637b96a137da4747ae3a5d48b80551ca
Quellennotizuspto-grants-2014_10