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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25859Generated: October 26, 2026

1-Benzyl-3-bromobenzene → 4-(3'-Benzylphenyl)-3-(S)-iso-propyl-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/25859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-3-bromobenzeneHCID 597532—
ReactantDichloromethane methanolHCID 21226129—
ReactantSodium t-butoxideHCID 23676156—
Reactant(S)-1-Boc-3-isopropylpiperazineHCID 24820348—
Catalyst2'-(diphenylphosphanyl)-N,N-dimethyl-[1,1'-biphenyl]-2-amineHCID 2734939—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product4-(3'-Benzylphenyl)-3-(S)-iso-propyl-piperazine-1-carboxylic acid tert-butyl esterHCID 6912986959,322%

Reaction Conditions

Temperature80 °C

Reaction Steps

9.4 mg (10.3 μmol, 0.013 eq.) Pd2(dba)3 and 11.4 mg (29.9 μmol, 0.04 eq.) 2-Diphenylphosphino-2′-dimethylamino-biphenyl were dissolved in 6 ml dry toluene. Then 170.7 mg (1.78 mmol, 2.32 eq.) NaOt-Bu was added, followed by a solution of 175.0 mg (0.77 mmol) 3-(S)-Isopropyl-piperazine-1-carboxylic acid tert-butyl ester (85) and 290.6 mg (1.18 μmol, 1.54 eq.) 1-Benzyl-3-bromo-benzene (87). The resulting mixture was heated at 80° C. for 22 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 (3+1)) yielded 276.5 mg (0.70 mmol, 91.49%) 4-(3′-Benzylphenyl)-3-(S)-iso-propyl-piperazine-1-carboxylic acid tert-butyl ester (88).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858600B2
Source datasetuspto-grants-2005_02
ORD IDord-f3e25a85adf64b2aa5d09bac8840401a
Source noteuspto-grants-2005_02