HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → methyl N-(tert-butoxycarbonyl)-4-nitrophenylalaninate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-propionic acid | HCID 118071 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | methyl N-(tert-butoxycarbonyl)-4-nitrophenylalaninate | HCID 14054107 | — |
Reaction Steps
To a mixture of the compound (1.15 g) obtained in Example 63, diethyl ether (6 ml) and methanol (14 ml), a solution of trimethylsilyldiazomethane in n-hexane (2.0 M, 7.4 ml) was added and the resulting mixture was stirred at room temperature for 16 h. The reaction solution was concentrated under reduced pressure to give the titled compound quantitatively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06534546B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-9fa620512cd443db8e95b83657de6408 |
| Source note | uspto-grants-2003_03 |