HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boc-L-Valine → Tert-butoxycarbonylalanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boc-L-Valine | HCID 83693 | — |
| Reactant | Benzyloxycarbonyl-L-proline | HCID 101987 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Tert-butoxycarbonylalanine | HCID 85082 | — |
Reaction Steps
Substantially the same procedure as described above was repeated except that N-t-BOC-L-valine (→P8) was used in place of the L-phenylalanine derivative. When N-CBZ-L-proline was used as starting material the deprotection was done by overnight hydrogenation with H2, 10% Pd/C in EtOH (→P9). In case of N-t-BOC-L-alanine the free amine was obtained after evaporation of the solvents and stirring the residue with saturated NaHCO3 solution (→P10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663174 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-d2561befc9224a639fd648a954bf6c19 |
| Source note | uspto-grants-1997_09 |