HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396871Generated: October 29, 2026
tert-Butyl bromoacetate → 1-Acetyl-3-benzylidene piperazine-2,5-dione N-butyl acetate
https://huagongshe.com/reaction/396871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | 1-Acetyl-3-benzylidene-2,5-piperazinedione | HCID 3759653 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Acetyl-3-benzylidene piperazine-2,5-dione N-butyl acetate | HCID 131724039 | 114.6% |
Reaction Steps
To a solution containing 6.36. g (26.00 mmol) of 1-Acetyl-3-benzylidene piperazine-2,5-dione described by D. Villemn, et al. (Synthetic Communications, 20:3325 (1990)), in 100 mL of DMF under nitrogen atmosphere was added 9.62 mL (65.10 mmol) of t-butyl bromoacetate and 7.55 g (32.60 mmol) of silver oxide. The reaction was heated to 45° C. overnight. The reaction was filtered through a plug of celite and the filtrate concentration under reduced pressure. The residue was diluted with ethyl acetate and washed with water. The organic phase was dried over magnesium sulfate. Filtration, removal of solvent under reduced pressure and column chromatography of the residue on silica gel with 1% methanol/dichloromethane gave 5.37 g of a tan solid. Further purification via preparative HPLC gave 2.5 g (27%) of the title compound. FAB MS [M+H] m/z: Calcd: 359, Found: 359.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06608175B2 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-e8159846992f457fb8b36e2973cbebb9 |
|---|
| Source note | uspto-grants-2003_08 |
|---|