HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl L-leucinate → N-t-butoxycarbonylglycyl-L-leucine benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl L-leucinate | HCID 6451313 | — |
| Reactant | t-Butoxycarbonylglycine-2,4,5-Trichlorophenyl Ester | HCID 12799284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-t-butoxycarbonylglycyl-L-leucine benzyl ester | HCID 53703413 | — |
Reaction Steps
A solution of 19.5 parts N-t-butoxycarbonylglycine 2,4,5-trichlorophenyl ester and 11.1 parts L-leucine benzyl ester in 200 parts methylene chloride is stirred overnight at room temperature. The solvent is then removed by evaporation under reduced pressure. The crude dipeptide is then subjected to low-pressure column chromatography on silica gel to afford N-t-butoxycarbonylglycyl-L-leucine benzyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04092304 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-0ac71ffc126449cab9a5591baaaff651 |
| Source note | uspto-grants-1978_05 |