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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922380Generated: October 26, 2026

Benzyl 4-propionylpiperazine-1-carboxylate → 1-(Piperazin-1-yl)propan-1-one

https://huagongshe.com/reaction/922380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-propionylpiperazine-1-carboxylateHCID 22596214—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(Piperazin-1-yl)propan-1-oneHCID 384437593%

Reaction Steps

A Parr shaker bottle was charged with a suspension of benzyl 4-propionylpiperazine-1-carboxylate (16), 10% palladium on carbon, 50% wet (900 mg) and absolute ethanol (100 mL). The Parr bottle was filled with 20 psi of hydrogen and shook for 3 h at rt. The resulting suspension was filtered through Celite and concentrated to yield the title compound (4.31 g, 93%) as a clear, colorless oil: 1H NMR (500 MHz, CDCl3) δ 3.75-3.63 (m, 2H), 3.48-3.42 (m, 2H), 2.87-2.80 (m, 4H), 2.34 (q, J=7.5 Hz, 2H), 1.98 (br s, 1H), 1.15 (t, J=7.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278940B2
Source datasetuspto-grants-2016_03
ORD IDord-64636ef78e1d454c98d7a2960ae70958
Source noteuspto-grants-2016_03