HuagongsheHuagongshe Chemistry Print Report · For research reference only
methyl O-benzyl-L-serylglycinate trifluoroacetate → 3-(Benzyloxymethyl)piperazine-2,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | methyl O-benzyl-L-serylglycinate trifluoroacetate | HCID 66584220 | — |
| Solvent | Triethylamine methanol | HCID 22728368 | — |
| Product | 3-(Benzyloxymethyl)piperazine-2,5-dione | HCID 66582436 | 68.4% |
Reaction Steps
A 250 ml, round-bottomed flask was charged with methyl O-benzyl-L-serylglycinate trifluoroacetate (9.37 g, 24.64 mmol) and 3:1 MeOH/triethylamine (50 mL). The mixture was then heated to reflux for 16 h. The reaction was then cooled to room temperature, concentrated, and diluted with ice cold 50% aqueous EtOH (50 mL). The resulting precipitate was collected by filtration and dried under reduced pressure to give 3-(benzyloxymethyl)piperazine-2,5-dione (3.95 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431563B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-28d1c17c80384a7698fc7ce7221edbff |
| Source note | uspto-grants-2013_04 |