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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376676Generated: October 30, 2026

Piperazine → 1-(2,5-Dimethoxyphenyl)piperazine

https://huagongshe.com/reaction/2376676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantCesium carbonateHCID 10796—
ReactantBenzene, 2-bromo-1,4-dimethoxy-HCID 91353—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product1-(2,5-Dimethoxyphenyl)piperazineHCID 275847348.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

1.98 g of piperazine, 1.0 g of 1-bromo-2,5-dimethoxybenzene, 800 mg of 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene, 310 mg of palladium(II) acetate and 2.25 g of cesium carbonate are dissolved in 30 ml of 1,4-dioxane and stirred at 100° C. under an argon atmosphere for 24 hours. The reaction mixture is extracted with 50 ml of saturated sodium bicarbonate solution and 50 ml of saturated sodium chloride solution, and the combined aqueous phases are basified with 2N sodium hydroxide solution and extracted five times with 50 ml of dichloromethane each time. The combined organic phases are dried over MgSO4 and then the solvent is removed in vacuo. 500 mg of 1-(2,5-dimethoxyphenyl)piperazine are obtained as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468369B2
Source datasetuspto-grants-2008_12
ORD IDord-7e195da5ae02465bbb10dd0110b8dee8
Source noteuspto-grants-2008_12