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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276114Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantAnisoleHCID 7519—
Reactant2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine t-butyl esterHCID 54481559—
CatalystMercuric acetateHCID 15337—
SolventDichloromethaneHCID 6344—
Product2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanineHCID 1554874058.2%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352976B1
Source datasetuspto-grants-2002_03
ORD IDord-5ae5529245274703a3c1f8b6e322927e
Source noteuspto-grants-2002_03