HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Aspartic Acid → N-(Benzyloxycarbonyl)aspartic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Aspartic Acid | HCID 5960 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Product | N-(Benzyloxycarbonyl)aspartic acid | HCID 2723942 | — |
Reaction Steps
The amino group of L-aspartic acid was protected as in Example 2 using benzyl chloroformate, to form N-benzyloxycarbonyl-L-aspartic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04941992 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-afcfe010b7ad40c5a3d8c39820c3ccb7 |
| Source note | uspto-grants-1990_07 |