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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912399Generated: November 1, 2026

Bromobenzene → Piperazine, 1-methyl-4-phenyl-

https://huagongshe.com/reaction/912399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
Reactant1-MethylpiperazineHCID 53167—
ReactantPotassium tert-butoxideHCID 23665647—
ProductPiperazine, 1-methyl-4-phenyl-HCID 20099174.4%

Reaction Steps

A 1 L flask was charged with 141.3 g of bromobenzene, 30.1 g of 1-methylpiperazine and 43.8 g of potassium tert-butoxide. The flask was then placed on an ice bath for 10 minutes and the contents rapidly stirred. 2.04 g of “PEPPSI” catalyst[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)-palladium (II) dichloride was then added and the flask fitted with a reflux condenser. The reaction was refluxed under a nitrogen atmosphere for 2 hours and then cooled to room temperature. The reaction mixture was then filtered through a pad of 800 mL of silica gel in a 2 L D-filter flask and the pad subsequently rinsed with 600 mL of ether. Then the product was extracted from the pad with ethanol. Evaporation of the ethanol gave 39.4 g of 1-methyl-4-phenylpiperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08025863B2
Source datasetuspto-grants-2011_09
ORD IDord-b3f6546dccf24fc48cf06ac33f43e005
Source noteuspto-grants-2011_09