HuagongsheHuagongshe Chemistry Print Report · For research reference only
beta-benzyl N-benzyloxycarbonyl-L-aspartyl-D-alanine amide → L-aspartyl-D-alanine amide monohydrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | beta-benzyl N-benzyloxycarbonyl-L-aspartyl-D-alanine amide | HCID 53846268 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | L-aspartyl-D-alanine amide monohydrate | HCID 22796342 | — |
Reaction Steps
To a solution of 61.10 parts of β-benzyl N-benzyloxycarbonyl-L-aspartyl-D-alanine amide in 800 parts by volume of 75% acetic acid is added 6 parts of palladium black metal catalyst, and the resulting mixture is shaken with hydrogen at room temperature at atmospheric pressure for about 6.5 hours. The catalyst is removed by filtration, and the solvents removed by distillation under reduced pressure to obtain an oil. This oil is triturated with water and stripped under reduced pressure three times to afford a solid. The solid is then triturated with ethanol, filtered, and dried under vacuum to yield L-aspartyl-D-alanine amide monohydrate. This product is represented by the following structural formula.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04012367 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-04d882ec8cb74848a57baf6434412d8b |
| Source note | uspto-grants-1977_03 |