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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737132Generated: October 27, 2026

Toluene → (S)-3-Benzyl-1-(2',5'-dimethyl-biphenyl-4-ylmethyl)-piperazine

https://huagongshe.com/reaction/737132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant(2,5-Dimethylphenyl)boronic acidHCID 2734347—
Reactant3-(S)-benzyl-1-(4-bromobenzyl)-piperazineHCID 57849462—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product(S)-3-Benzyl-1-(2',5'-dimethyl-biphenyl-4-ylmethyl)-piperazineHCID 5784948637%

Reaction Conditions

Temperature85 °C

Reaction Steps

0.1 g of 3-(S)-benzyl-1-(4-bromo-benzyl)-piperazine were combined with 1.5 equiv. of 2,5-dimethylphenyl boronic acid, 0.05 equiv. of tetrakis(triphenylphosphine)palladium(0), 6 equiv. of 2M aqueous sodium carbonate solution, toluene and ethanol. The reaction mixture was heated at 85° C. under nitrogen overnight. The reaction mixture was concentrated in vacuo. The residue was diluted with water and extracted with ethyl acetate. The combined organic phases were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was purified by flash chromatography to afford 0.04 g of the title compound. Yield 37% ES MS (+) m/z 371.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595397B2
Source datasetuspto-grants-2009_09
ORD IDord-38f8ce7570524cb68d505c5fcaaf192a
Source noteuspto-grants-2009_09