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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972725Generated: November 2, 2026

1-Benzyl-4-(cyclopropylcarbonyl)piperazine → 1-(Cyclopropylcarbonyl)piperazine

https://huagongshe.com/reaction/1972725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(cyclopropylcarbonyl)piperazineHCID 1220050—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(Cyclopropylcarbonyl)piperazineHCID 206423597%

Reaction Steps

10% Palladium on carbon (175 mg, 10% by wt.) was placed under an inert atmosphere and suspended in EtOH (5 mL). A solution of (4-benzyl-piperazin-1-yl)-cyclopropyl-methanone (1.75 g, 7.16 mmol) dissolved in EtOH (25 mL) was added. The reaction mixture was placed under H2 atmosphere (1 atmosphere pressure) and stirred overnight. The resulting mixture was filtered through a pad of Celite® and the solvent was concentrated in vacuo to give 1.07 g (97%) of the title compound as a clear oil. 1H-NMR (300 MHz, CD3OD) 3.74 (broad s, 2H), 3.57 (broad s, 2H), 2.87 (broad s, 2H), 2.80 (broad s, 2H), 1.97 to 1.91 (m, 1H), 0.89 to 0.78 (m, 4H); ES-MS m/z 154.9 [M+H]+, RT (min) 1.02.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-ba99f7e8a90a4003a7048ff6a6fc849b
Source noteuspto-grants-2013_04