HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → (S)-Benzyl (tetrahydro-2,5-dioxo-3-furyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | N-(Benzyloxycarbonyl)aspartic acid | HCID 2723942 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (S)-Benzyl (tetrahydro-2,5-dioxo-3-furyl)carbamate | HCID 11128682 | — |
Reaction Steps
For example, N-benzyloxycarbonyl-L-aspartic acid is dissolved in a large excess of acetic anhydride, the acetic acid formed by the reaction and the excess acetic anhydride are distilled off under reduced pressure and the effect of any acetic acid remaining in the residue is removed by the addition of an organic solvent to give N-benzyloxycarbonyl-L-aspartic anhydride [J. Am. Chem. Soc., 81, 167-173 (1959)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05302743 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-0d00a997b1df4e23a14cef71c9b78832 |
| Source note | uspto-grants-1994_04 |