HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(t-butyloxycarbonyl)methyl-N-t-butyloxycarbonyl-D-leucine benzyl ester → N-(t-butyloxycarbonyl)methyl-N-t-butyloxycarbonyl-D-leucine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(t-butyloxycarbonyl)methyl-N-t-butyloxycarbonyl-D-leucine benzyl ester | HCID 86700985 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(t-butyloxycarbonyl)methyl-N-t-butyloxycarbonyl-D-leucine | HCID 86700984 | 99.7% |
Reaction Steps
N-(t-butyloxycarbonyl)methyl-N-t-butyloxycarbonyl-D-leucine benzyl ester (2.1 g) was dissolved in methanol (25 ml), and 10% palladium-carbon (210 mg) was added. The resulting mixture aerated with hydrogen was allowed to react at room temperature for 3 h, filtered and concentrated under reduced pressure to remove the solvent to give a colourless oil (1.66 g, 96%), which was directly used for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434760B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-f2c8c4aa22584e9eb0091ea75c82d0c9 |
| Source note | uspto-grants-2016_09 |