Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25861Generated: October 25, 2026

o-Bromocumene → 1-(3-Benzyl-phenyl)-2-(S)-isopropyl-4-(2-isopropyl-phenyl)-piperazine

https://huagongshe.com/reaction/25861

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-BromocumeneHCID 23475—
ReactantDimethoxyethane ethanolHCID 20074477—
Reactant4-(3'-Benzylphenyl)-3-(S)-isopropyl-piperazineHCID 20760004—
ReactantSodium t-butoxideHCID 23676156—
Catalyst2'-(diphenylphosphanyl)-N,N-dimethyl-[1,1'-biphenyl]-2-amineHCID 2734939—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product1-(3-Benzyl-phenyl)-2-(S)-isopropyl-4-(2-isopropyl-phenyl)-piperazineHCID 6912955562.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

110.7 mg (0.38 mmol) 4-(3′-Benzylphenyl)-3-(S)-isopropyl-piperazine (88a), 123.5 mg (0.62 mmol, 1.65 eq.) 1-Bromo-2-isopropyl-benzene 11.7 mg (12.7 μmol, 0.034 eq.) Pd2(dba)3, 7.4 mg (19.3 μmol, 0.05 eq.) 2-Diphenylphosphino-2′-dimethylamino-biphenyl and 87.3 mg (0.91 mmol, 2.42 eq.) NaOt-Bu were dissolved in 5 ml dry toluene. The resulting mixture was heated under N2 at 80° C. for 15.5 h. After cooling to room temperature the mixture was diluted with ether and washed with brine. The comb. org. fractions were dried over Na2SO4 and evaporated. Column chromatography (hexanes/EtOAc (9+1)) yielded 96.5 mg (0.23 mmol, 62.20%) 1-(3-Benzyl-phenyl)-2-(S)-isopropyl-4-(2-isopropyl-phenyl)-piperazine (89) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858600B2
Source datasetuspto-grants-2005_02
ORD IDord-1b122892a0f943948cd06552bfdb562e
Source noteuspto-grants-2005_02