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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361440Generated: October 25, 2026

Piperazine → 1-(2-Chloro-4-fluorophenyl)piperazine

https://huagongshe.com/reaction/1361440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantBinap, (A+-)-HCID 634876—
Reactant1-Bromo-2-chloro-4-fluorobenzeneHCID 2733406—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product1-(2-Chloro-4-fluorophenyl)piperazineHCID 18423151—

Reaction Conditions

Temperature120 °C

Reaction Steps

A suspension of 1-bromo-2-chloro-4-fluorobenzene (4.19 g, 20 mmoles), piperazine (10.32 g, 120 mmoles), sodium tert-butoxide (2.3 g, 1.5 mmoles), tris(dibenzylideneacetone)dipalladium (366 mg, 0.4 mmoles) and racemic (−)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (747 mg, 1.2 mmoles) in toluene (2 mL) was heated to 120° C. overnight. The mixture was cooled, filtered and the filtrate concentrated under reduced pressure. The crude residue was purified by column chromatography (silica gel, 0-5% 2N methanolic ammonia in DCM) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880001B2
Source datasetuspto-grants-2011_02
ORD IDord-ddc7e461a1fe4f839bf012a6fe8b1db8
Source noteuspto-grants-2011_02