HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(Benzyloxycarbonyl)aspartic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 53782664 | HCID 53782664 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(Benzyloxycarbonyl)aspartic acid | HCID 2723942 | — |
| Product | (S)-Benzyl (tetrahydro-2,5-dioxo-3-furyl)carbamate | HCID 11128682 | — |
Reaction Steps
Suitable amount of sample was withdrawn from the uniform reaction mixture thus obtained and dissolved in a methanol solution containing 5% by weight of triethylamine. α- and β-Isomers of N-benzyloxycarbonylcarbobenzoxy-L-aspartic acid methyl ester formed by the reaction of N-benzyloxycarbonyl-L-aspartic anhydride with methanol and residual N-benzyloxycarbonyl-L-aspartic acid were determined by high performance liquid chromatography. The content and yield of N-benzyloxycarbonyl-L-aspartic anhydride were calculated from measured values. Results are shown in Table 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05302743 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-ad6fd93f35f34c2fa8bf7db19abbb2e4 |
| Source note | uspto-grants-1994_04 |