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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885880Generated: October 26, 2026

Benzaldehyde → 1-[4-(4-Benzylpiperazin-1-yl)phenyl]ethanone

https://huagongshe.com/reaction/885880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPiperazin-4-ylacetophenoneHCID 97269—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventEthyl AcetateHCID 8857—
Product1-[4-(4-Benzylpiperazin-1-yl)phenyl]ethanoneHCID 75780854.1%

Reaction Steps

A mixture of 1-(4-piperazin-1-yl-phenyl)-ethanone (500 mg, 2.45 mmol), benzaldehyde (312 mg, 2.94 mmol) and NaBH(OAc)3 (778 mg, 3.67 mmol) in AcOEt (15 ml) was stirred at room temperature overnight. The resulting solution was partitioned between water and DCM and the organic phase was dried over Na2SO4 and evaporated in vacuo. The crude product was purified by silica gel chromatography (eluent: DCM/MeOH/NH4OH 95:5:0.2) to give 390 mg of 1-[4-(4-benzyl-piperazin-1-yl)-phenyl]-ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242175B2
Source datasetuspto-grants-2012_08
ORD IDord-b8e8179a00464bc988c4bee90f5f1b3b
Source noteuspto-grants-2012_08