HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(tert-butoxycarbonyl)-L-aspartic acid → (S)-tert-Butyl (2,5-dioxotetrahydrofuran-3-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(tert-butoxycarbonyl)-L-aspartic acid | HCID 99718 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-tert-Butyl (2,5-dioxotetrahydrofuran-3-yl)carbamate | HCID 13657126 | — |
Reaction Steps
To a solution of 23.3 g N-t-butyloxycarbonyl-L-aspartic acid in 150 mL of tetrahydrofuran was added portionwise 20.6 g of N,N-dicyclohexyl-carbodiimide at 0° C. and overnight at room temperature. The precipitated dicyclohexyl urea was filtered off and all solvent was evaporated under reduced pressure. The oily residue was crystallized from acetone/hexane to give 18.24 g of anydride as white needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008058 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-671e327625df43ec844fd6ebc60ff142 |
| Source note | uspto-grants-1999_12 |