HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429753Generated: October 31, 2026
Morpholine → N-[N-benzyloxycarbonyl-L-prolyl]morpholine
https://huagongshe.com/reaction/429753
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | Benzyloxycarbonyl-L-proline | HCID 101987 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[N-benzyloxycarbonyl-L-prolyl]morpholine | HCID 13564348 | 69.5% |
Reaction Steps
A solution of N-benzyloxycarbonyl-L-proline (5 g, 20.06 mmol), morpholine (1.92 ml, 20.06 mmol), and N-hydroxysuccinimide (2.31 g, 20.06 mmol) in N, N-dimethylformamide (100 ml) was added DCC (4.14 g, 20.06 mmol) and the resulting mixture was stirred for 4 h at room temperature. After the precipitation was filtered off, the filtrate was concentrated in vacuo. The residue was dissolved in ethyl acetate and the resulting precipitation was filtered off. After the filtrate was washed with dilute hydrochloric acid, saturated sodium hydrogencarbonate aq., and water, the organic layer was dried over magnesium sulfate and concentrated in vacuo. The residue was crystallized from the mixed solvents of ethyl acetate-hexane to give the compound (34) (4.44 g, 69.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06319902B1 |
|---|
| Source dataset | uspto-grants-2001_11 |
|---|
| ORD ID | ord-918a80e19f184c84a99dbd9be477e862 |
|---|
| Source note | uspto-grants-2001_11 |
|---|