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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888192Generated: October 27, 2026

Methane → (3R)-1-(3,4-dimethoxyphenyl)-3-methylpiperazine

https://huagongshe.com/reaction/888192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantBenzene, 4-bromo-1,2-dimethoxy-HCID 76114—
ReactantBinap, (A+-)-HCID 634876—
Reactant2-Methylpiperazine, (R)-HCID 7330434—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventEthyl ether methylene chlorideHCID 21881112—
Product(3R)-1-(3,4-dimethoxyphenyl)-3-methylpiperazineHCID 5848795928.1%

Reaction Steps

A mixture of (R)-(−)-2-methylpiperazine (2.0 g, 20 mmol), 4-bromo-1,2-dimethoxybenzene (4.33 g, 20 mmol) and sodium tert-butoxide (2.88 g, 30 mmol) was prepared in anhydrous toluene (50 mL). The solution was degassed by argon bubbling for 10 min. Then palladium(II) acetate (220 mg, 1 mmol) and (+/−)-BINAP (500 mg, 0.8 mmol) were added. The resulting mixture was heated at reflux for 4 hours. Then the reaction mixture was cooled to RT and diluted with Et2O (50 mL). The salts were removed by filtration on Celite and the solvents were removed under reduced pressure to give a dark brown oil. Purification by flash chromatography (CHCl3/MeOH) gave a brown oil. This oil was taken up with DCM/Et2O, treated with activated charcoal at RT for 10 min and filtered on Celite. The solvents were removed under reduced pressure to give 1.33 g (28%) of the title compound as a yellow oil. M+(ESI): 237.2. HPLC (Condition A), Rt: 1.2 min (HPLC purity: 93.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247437B2
Source datasetuspto-grants-2012_08
ORD IDord-58c24ae48d46400eae0168ce3df705c7
Source noteuspto-grants-2012_08