HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276111Generated: October 25, 2026
Cesium carbonate → 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester
https://huagongshe.com/reaction/276111
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Methoxy-alpha-toluenethiol | HCID 80407 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 2-bromopentanoyl-(L)-homophenylalanine methyl ester | HCID 22950831 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester | HCID 22950828 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06352976B1 |
|---|
| Source dataset | uspto-grants-2002_03 |
|---|
| ORD ID | ord-d1385ca9dc824c218ae0cd8094c64e04 |
|---|
| Source note | uspto-grants-2002_03 |
|---|