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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287639Generated: October 29, 2026

Sodium Iodide → 1-[4-(4-Ethylphenyl)piperazin-1-yl]-3-[2-oxopyrrolidin-1-yl]propane

https://huagongshe.com/reaction/2287639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactant1-(4-Ethylphenyl)piperazineHCID 3265804—
Reactant1-(3-Chloropropyl)pyrrolidin-2-oneHCID 11105662—
SolventDimethylformamideHCID 6228—
Product1-[4-(4-Ethylphenyl)piperazin-1-yl]-3-[2-oxopyrrolidin-1-yl]propaneHCID 9926922—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-chloro-3-[2-oxopyrrolidin-1-yl]propane (2.0 g, 12.0 mmol), 1-(4-ethylphenyl)piperazine (2.36 g, 12.0 mmol), anhydrous Na2CO3 (0.658 g, 6.2 mmol) and NaI (0.18 g, 1.2 mmol) in dry DMF (10 ml) was stirred at 80° C. for 12 hrs. The reaction mixture was cooled, poured on water (30 ml) and the separated residue was extracted with CHCl3 (2×30 ml). The extracts were dried over Na2So4 and concentrated under reduced pressure to give 1-[4-(4-ethylphenyl)piperazin-1-yl]-3-[2-oxopyrrolidin-1-yl]propane as an oil which was purified by flash column chromatography over silica gel using chloroform as eluent, yield 2.43 g (62.0%). IR (Neat): 2940, 2800, 1660, 1440, 1000, 900,800. 1H NMR (CDCl3): 1.20(t, 3H, J=6.0 Hz, CH2CH3, 1.60-280(m, 14H, 3',4',2,1 & 2×N--CH2, CH2CH3), 3.00-3.60(m, 8H, 5', 3 & 2×N--CH2). MS: m/z 315 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06084097
Source datasetuspto-grants-2000_07
ORD IDord-55f6c080f2cc47d8ad654f88a3283364
Source noteuspto-grants-2000_07