HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596741Generated: October 30, 2026
p-Toluenesulfonic acid → Boc-Gly-Phe-Gly-OBzl
https://huagongshe.com/reaction/1596741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | Phe-Gly-OBzl | HCID 91977316 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Boc-Gly-Phe-Gly-OBzl | HCID 131722860 | 65.5% |
Reaction Steps
A mixture of p-toluenesulfonic acid salt of Phe-Gly-OBzl (3.06 g), Boc-Gly-OH (1.10 g), N-hydroxysuccinimide (941 mg), N-methylmorpholine (0.725 ml), and N,N-dimethylformamide (40 ml) was cooled to 4° C., and added with N,N′-dicyclohexylcarboduimide (1.56 g). The mixture was allowed to react overnight at room temperature with stirring, and then evaporated to dryness under reduced pressure. The residue was purified by silica gel column chromatography (eluent: dichloromethane:methanol=98:2 solution) to give Boc-Gly-Phe-Gly-OBzl (1.93 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06291671B1 |
|---|
| Source dataset | uspto-grants-2001_09 |
|---|
| ORD ID | ord-77c4d787024c4c1e91b0d5a0e0505439 |
|---|
| Source note | uspto-grants-2001_09 |
|---|