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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297590Generated: October 30, 2026

1-Tert-butylpiperazine → 1-Phenylpiperazine

https://huagongshe.com/reaction/2297590

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butylpiperazineHCID 3530572—
Reactant1-Bromo-2-butoxybenzeneHCID 19008126—
ReactantSodium t-butoxideHCID 23676156—
CatalystBinap, (A+-)-HCID 634876—
SolventTolueneHCID 1140—
Product1-PhenylpiperazineHCID 7096157.1%

Reaction Steps

Part A: To a solution of n-butyloxybromobenzene (5.00 g, 21.82 mmol) in toluene (50 mL) was added tert-butyl piperazine (4.88 g, 26.18 mmol) and sodium tert-butoxide (2.94 g, 30.55 mmol). After stirring at ambient temperature for several minutes, BINAP (0.408 g, 0.655 mmol) and tris(dibenzyldeneacetone)-dipallidium (0) (0.200 g, 0.218 mmol) were added. The resulting mixture was heated to eighty degrees Celsius for 21 hours. After cooling to ambient temperature, the reaction mixture was filtered through a pad of Celite®, washing with diethyl ether and dichloromethane. Chromatography (on silica, ethyl acetate/hexanes) provided the phenyl-piperazine as a tan solid (5.56 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492367B1
Source datasetuspto-grants-2002_12
ORD IDord-57d6173298034604bd9735ba369e20f5
Source noteuspto-grants-2002_12