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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274842Generated: November 3, 2026

Piperazine → 1-(1-Naphthyl)piperazine

https://huagongshe.com/reaction/1274842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-BromonaphthaleneHCID 7001—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantPotassium tert-butoxideHCID 23665647—
Catalystpalladium(II) acetateHCID 167845—
SolventDichloromethaneHCID 6344—
SolventO-XyleneHCID 7237—
Product1-(1-Naphthyl)piperazineHCID 134242%

Reaction Steps

83.2 g (966 mM [sic]) of piperazine, 38.0 g (339 mM [sic]) of potassium tert-butoxide and 50.0 g (241 mM [sic]) of 1-bromonaphthalene were added to a mixture of 5.4 g (24.2 mM [sic]) of palladium acetate and 14.7 g (48.3 mM [sic]) of tri-o-tolylphosphine in 500 ml of xylene, and the mixture was refluxed while stirring vigorously under a nitrogen atmosphere for 10 h. The mixture was then diluted with methylene chloride, the insoluble residues were filtered off, and the filtrate was concentrated. The crude product was purified by column chromatography (silica gel, eluent THF/methanol/ammonia 85/13/2). 21.5 g (42%) of product were isolated with melting point 84-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159962
Source datasetuspto-grants-2000_12
ORD IDord-8dab580654ff4178af892408a29410bd
Source noteuspto-grants-2000_12