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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278615Generated: October 31, 2026

1,3-Dibromopropane → HCID 14364333, compound

https://huagongshe.com/reaction/1278615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantSodium hydrideHCID 24758—
Reactant5-Methyl-2-pyrrolidoneHCID 66055—
ReactantHCID 18430921HCID 18430921—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14364333HCID 14364333—
ProductHCID 70151694HCID 70151694—

Reaction Steps

1-[3-(4-Benzyl-1-piperazinyl)propyl]-5-methyl-2-pyrrolidinone A solution of 5-methyl-2-pyrrolidinone (0.99 g/10.0 mmol) in tetrahydrofuran (10 ml) was added to a suspension of sodium hydride(60% in oil, 0.6 g/1 5.0 mmol) in tetrahydrofuran (50 ml) at 0° C. and the resulting mixture was stirred for 1 hour at ambient temperature. To the mixture was added a solution of 1,3-dibromopropane (5.1 ml/50.0 mmol) in tetrahydrofuran (10 ml) and the mixture was stirred for 1 day. The mixture was poured into water (50 ml) and extracted with ethyl acetate (50 ml×2). The combined extracts were washed with brine (50 ml), dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (Si, 230-400 mesh/dichloromethane:methanol=30:1) to give as a mixture of 1-(3-bromoproyl)-5-methyl-2-pyrrolidinone and 1-allyl-5-methyl-2-pyrrolidinone (0.8 g). The mixture was dissolved with ethanol (5 ml). To the solution was added 1-benzylpiperazine (0.4 mV/2.19 mmol), and the mixture was stand for 7 days. The solvent was removed in vacuo. The residue was dissolved in dichloromethane (20 ml) and 2N-NaOH (20 ml). The aqueous layer was extracted with dichloromethane (20 ml). The combined extracts were washed with brine (20 ml), dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (Si, 230-400 mesh/dichloromethane:methanol=30:1-15:1) to give as the titled compound (0.59 g/19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444677B2
Source datasetuspto-grants-2002_09
ORD IDord-45064d72acd546e9b8854ea56eb66411
Source noteuspto-grants-2002_09