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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432018Generated: October 29, 2026

1-(2-Methoxyphenyl)piperazine → 4-[4-(2-Methoxyphenyl)piperazin-1-yl]-1,2-diphenylbutan-1-one

https://huagongshe.com/reaction/432018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantSodiumHCID 5360545—
ReactantHCID 12018120HCID 12018120—
SolventDichloromethaneHCID 6344—
Product4-[4-(2-Methoxyphenyl)piperazin-1-yl]-1,2-diphenylbutan-1-oneHCID 1552402595%

Reaction Steps

The 3-benzoyl-3-phenylpropionaldehyde residue obtained from Step B, above, (˜8.85 mmol) was dissolved in 110 mL of methylene chloride. To this solution was added 2-methoxyphenylpiperazine (10.61 mmol) and sodium triacetoxyboranehydride, NaBH(OAc)3, (10.61 mmol). The mixture was stirred at room temperature for 3 hours. Aqueous workup followed by flash chromatography gave pure product 1-(2-methoxyphenyl)-4-[3-(benzoyl)-3-(phenyl)propyl]piperazine (3.48 g) in 95% yield for last two steps. One equivalent of oxalic acid was added to the free base dissolved in methanol. The solvent was evaporated and the product was dried under vacuum to form the oxalate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660859B2
Source datasetuspto-grants-2003_12
ORD IDord-a7c3e31f07f94449bd06179c0fcf1ad1
Source noteuspto-grants-2003_12