Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288596Generated: October 29, 2026

Potassium Iodide → HCID 3994476, compound

https://huagongshe.com/reaction/2288596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2-Methoxyphenyl)piperazine hydrochlorideHCID 9899402—
ReactantHCID 22645908HCID 22645908—
SolventDimethylformamideHCID 6228—
ProductHCID 3994476HCID 3994476—

Reaction Conditions

Temperature100 °C

Reaction Steps

Scheme-III: A mixture of 1-chloro-4-(2,5-dioxopyrrolidin-1-yl)butane (11.0 g, 58.04 mmol), 1-[2-methoxyphenyl)piperazin hydrochloride (12.99 g, 56.85 mmol), potassium carbonate (16.02 g, 116.09 mmol) and potassium iodide (0.577 g, 3.48 mmol) in N,N-dimethylformamide (45 ml) was stirred at 100° C. for 18 hours. N,N-dimethylformamide was evaporated at reduced pressure and the residue was taken up in water (100 ml) and extracted with chloroform (2×100 ml). The extracts were dried over Na2SO4 and concentrated under reduced pressure to give 1-[4-(2-methoxyphenyl)piperazine-1-yl]-4-(2,5-dioxopyrrolidin-1-yl)butane as an oil which was purified by column chromatography over silica gel (230-400 mesh) using chloroform-methanol (98.2) as eluent; yield 18.00 g, (92%), oil. Hydrochloride salt was prepared by the method described above; mp 218-220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090809
Source datasetuspto-grants-2000_07
ORD IDord-8fd4b4dfdeaf429eaac3604061734910
Source noteuspto-grants-2000_07