HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[2-(ethoxycarbonyl)ethyl]-N-t-butyloxycarbonyl-D-leucine benzyl ester → N-[2-(ethoxycarbonyl)ethyl]-N-t-butyloxycarbonyl-D-leucine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[2-(ethoxycarbonyl)ethyl]-N-t-butyloxycarbonyl-D-leucine benzyl ester | HCID 86700995 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[2-(ethoxycarbonyl)ethyl]-N-t-butyloxycarbonyl-D-leucine | HCID 86700994 | 93% |
Reaction Steps
N-[2-(ethoxycarbonyl)ethyl]-N-t-butyloxycarbonyl-D-leucine benzyl ester (837 mg) was dissolved in methanol (25 ml), and 10% palladium-carbon (90 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 (612 mg, 93%), 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-66d78d45530d44e598c266f77f2a0b67 |
| Source note | uspto-grants-2016_09 |