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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804412Generated: November 1, 2026

Benzene, 1-bromo-2,4-dimethyl- → HCID 67381065, compound

https://huagongshe.com/reaction/1804412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-bromo-2,4-dimethyl-HCID 68503—
Reactant(R)-1-Boc-3-methylpiperazineHCID 2756811—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 67381065HCID 67381065—

Reaction Steps

To a mixture of 1-bromo-2,4-dimethylbenzene (3.8 mL), (R)-4-N-Boc-2-methylpiperazine (5.0 g), palladium (II) acetate (281 mg), 2-(dicyclohexylphosphino)-2′,4′,6′-tri-isopropyl-1,1′-biphenyl (1.19 g) and sodium tert-butoxide (3.4 g) was added toluene (50 mL), and the mixture was refluxed for 3 hr. After cooling, the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The residue was purified by column chromatography (chloroform) to give (R)-4-(2,4-dimethylphenyl)-3-methylpiperazine-1-carboxylic acid tert-butyl ester. The compound was dissolved in chloroform (8.0 mL), 4N hydrogen chloride/ethyl acetate (8.0 mL) was added, and the mixture was stirred at room temperature overnight. The reaction mixture was alkalified, and extracted with chloroform. The organic layer was evaporated to give (R)-1-(2,4-dimethylphenyl)-2-methylpiperazine (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-2ffb9d8fdb4e4631ac0018c965279fc8
Source noteuspto-grants-2013_01