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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063310Generated: November 1, 2026

HCID 16123291, compound → 1-Propanone, 1-[4-(3-azetidinyl)-1-piperazinyl]-

https://huagongshe.com/reaction/2063310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 16123291HCID 16123291—
CatalystPalladium hydroxideHCID 9942167—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product1-Propanone, 1-[4-(3-azetidinyl)-1-piperazinyl]-HCID 16123293111.7%

Reaction Steps

1-[1-(diphenylmethyl)azetidin-3-yl]-4-propionylpiperazine (0.22 g, 0.59 mmol) was dissolved in a mixture of ethanol (9 mL) and acetic acid (0.2 mL) and to the resultant solution was added palladium hydroxide on carbon (83 mg). The mixture was stirred under hydrogen (5 bar) at RT for 23 h and then the catalyst was filtered off by means of a phase separator column then washing with ethanol. The solvent was removed by evaporation and the residue was dissolved in methanol (1 mL). The solution was filtered through a cation exchange column (Isolate SCX-2, 10 g). The column was washed with THF and then the product was eluted with ammonia-saturated methanol. The solvent was removed by evaporation and there was obtained 0.13 g (100%) of the title compound as an oil. 1H NMR (500 MHz, CD3OD): 1.1 (t, 3H), 2.3-2.5 (m, 6H), 3.4 (m, 1H), 3.6 (m, 4H), 3.9-4.0 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288370B2
Source datasetuspto-grants-2012_10
ORD IDord-c532d71fd93542f28940f30370de6003
Source noteuspto-grants-2012_10