HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine t-butyl ester | HCID 54481559 | — |
| Catalyst | Mercuric acetate | HCID 15337 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine | HCID 15548740 | 58.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06352976B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-5ae5529245274703a3c1f8b6e322927e |
| Source note | uspto-grants-2002_03 |