HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(Benzyloxycarbonyl)aspartylphenylalanine → L-Aspartyl-L-phenylalanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(Benzyloxycarbonyl)aspartylphenylalanine | HCID 11090974 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | L-Aspartyl-L-phenylalanine | HCID 93078 | — |
Reaction Steps
The lower alkyl ester of N-benzyloxycarbonyl-α-L-aspartyl-L-phenylalanine as the starting compound is dissolved in toluene and, as the reaction of elimination proceeds, the lower alkyl ester of α-L-aspartyl-L-phenylalanine as the product formed in the organic phase is transferred into the aqueous phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04564471 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-4411de06eae04c01a2100ada3f95d22f |
| Source note | uspto-grants-1986_01 |