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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978877Generated: November 1, 2026

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

https://huagongshe.com/reaction/1978877

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 numberUS06239135B1
Source datasetuspto-grants-2001_05
ORD IDord-29ff3337f9914b088319e39d5c2942c8
Source noteuspto-grants-2001_05