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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276112Erstellt: 26. Oktober 2026

Hydrochloric Acid → 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine

https://huagongshe.com/reaction/276112

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethanolHCID 887—
EduktLithium HydroxideHCID 3939—
Edukt2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl esterHCID 22950828—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produkt2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanineHCID 22950827—

Reaktionsschritte

Combine 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester (3.50 g, 8.15 mmol) and methanol (30 mL)and tetrahydrofuran (30 (mL). Cool in an ice bath. Add an aqueous 2M lithium hydroxide solution (8.2 mL, 16.4 mmol). After 18 hours, adjust the pH to about 6 using an aqueous 10% hydrochloric acid solution and evaporate in vacuo to give a residue. Partition the residue between dichloromethane and water, adjust the pH of the aqueous layer to about 1 using an aqueous 10% hydrochloric acid solution. Separate the layers, extract the aqueous layer repeatedly with ethyl acetate. Combine the organic layers, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 95% 1/1 hexane/ethyl acetate/5% acetic acid to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352976B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-222d2ac6f50248dabfb0e58127fe60d6
Quellennotizuspto-grants-2002_03