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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276111Erstellt: 25. Oktober 2026

Cesium carbonate → 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester

https://huagongshe.com/reaction/276111

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt4-Methoxy-alpha-toluenethiolHCID 80407—
EduktEthyl acetate hexaneHCID 21226206—
Edukt2-bromopentanoyl-(L)-homophenylalanine methyl esterHCID 22950831—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl esterHCID 22950828—

Reaktionsschritte

Combine 2-bromopentanoyl-(L)-homophenylalanine methyl ester (3.6 g, 10 mmol), 4-methyoxybenzylmercaptan (3.48 mL, 25 mmol), and tetrabutylammonium iodide (about 50 mg) in dimethylformamide (10 mL). Degas by repeatedly applying vacuum and filling the vessel with nitrogen. Add cesium carbonate (4.10 g, 12.5 mmol). After 15 hours, partition the reaction mixture between water and methyl t-butyl ether, saturate the aqueous layer with sodium chloride. Extract the aqueous layer with brine, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 4/1 hexane/ethyl acetate and then 2.5/1 hexane/ethyl acetate to give the title compound: Rf=0.44 (silica gel, 2.5/1 hexane/ethyl acetate).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352976B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-d1385ca9dc824c218ae0cd8094c64e04
Quellennotizuspto-grants-2002_03