HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376676Generated: October 30, 2026
Piperazine → 1-(2,5-Dimethoxyphenyl)piperazine
https://huagongshe.com/reaction/2376676
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Benzene, 2-bromo-1,4-dimethoxy- | HCID 91353 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(2,5-Dimethoxyphenyl)piperazine | HCID 2758473 | 48.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468369B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-7e195da5ae02465bbb10dd0110b8dee8 |
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| Source note | uspto-grants-2008_12 |
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