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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890983Generated: October 28, 2026

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

https://huagongshe.com/reaction/890983

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. m.p.=161-163° C.; MS (m/e): 414 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001908B2
Source datasetuspto-grants-2006_02
ORD IDord-96643e0da998456d9c0e7dbb025cfae5
Source noteuspto-grants-2006_02