Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276114Erstellt: 23. Oktober 2026

Carbon Tetrachloride → 2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine

https://huagongshe.com/de/reaction/276114

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon TetrachlorideHCID 5943—
EduktAnisoleHCID 7519—
Edukt2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine t-butyl esterHCID 54481559—
KatalysatorMercuric acetateHCID 15337—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanineHCID 1554874058,2%

Reaktionsschritte

Combine 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine t-butyl ester (0.20 g, 0.33 mmol), mercury (II) acetate (0.134 g, 0.42 mmol), and anisole (0.37 mL, 3.4 mmol) in dichloromethane (9 mL). Cool in an ice bath and degas by repeatedly applying vacuum and filling the vessel with nitrogen, Add trifluoroacetic acid (4 mL). After 1 hour, warm to ambient temperature. After 3 hours, purge with hydrogen sulfide (gas) for about 10 minutes. Filter and evaporate in vacuo to give a residue. Repeatedly, combine the residue and carbon tetrachloride and evaporate in vacuo to give a residue. Triturate the residue with hexane to give the title compound as a solid (85 mg, 57%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352976B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-5ae5529245274703a3c1f8b6e322927e
Quellennotizuspto-grants-2002_03