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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant1-Acetyl-3-benzylidene-2,5-piperazinedioneHCID 3759653—
CatalystSilver(II) oxideHCID 92152—
SolventDimethylformamideHCID 6228—
Product1-Acetyl-3-benzylidene piperazine-2,5-dione N-butyl acetateHCID 131724039114.6%

Reaction Conditions

Temperature45 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608175B2
Source datasetuspto-grants-2003_08
ORD IDord-e8159846992f457fb8b36e2973cbebb9
Source noteuspto-grants-2003_08