Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091378Generated: November 2, 2026

Dimethylformamide → 4-((2S)-1,4-dibenzylpiperazin-2-yl)benzaldehyde

https://huagongshe.com/reaction/1091378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant(2S)-1,4-dibenzyl-2-(4-bromophenyl)piperazineHCID 66594629—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-((2S)-1,4-dibenzylpiperazin-2-yl)benzaldehydeHCID 8663455741%

Reaction Steps

n-Butyllithium (1.56M in hexane, 14 ml, 21.8 mmol) was added to a solution of (2S)-1,4-dibenzyl-2-(4-bromophenyl)piperazine (6.1 g, 14.5 mmol) in tetrahydrofuran (60 ml) at −78° C. After one hour stirring, dimethylformamide (1.6 g, 21.9 mmol) was added and the solution was stirred for one hour. The mixture was partitioned between water and chloroform. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting 5-10% methanol in chloroform to furnish 4-((2S)-1,4-dibenzylpiperazin-2-yl)benzaldehyde (1.6 g, 41%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129377B2
Source datasetuspto-grants-2012_03
ORD IDord-e15847031e8e45eaa77ca1fcf6e68f9d
Source noteuspto-grants-2012_03