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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 199Generated: October 23, 2026

Piperazine → 1-(4-Benzyloxy-3-fluorophenyl)piperazine

https://huagongshe.com/en/reaction/199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-(Benzyloxy)-4-bromo-2-fluorobenzeneHCID 18757491—
ReagentSodium t-butoxideHCID 23676156—
CatalystBinap, (A+-)-HCID 634876—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product1-(4-Benzyloxy-3-fluorophenyl)piperazineHCID 2311148371.64%

Reaction Conditions

Temperature110 °C

Reaction Steps

sodium 2-methylpropan-2-olate (6.43 g, 66.88 mmol) was added to 1-(benzyloxy)-4-bromo-2-fluorobenzene (13.43 g, 47.77 mmol) and piperazine (24.69 g, 286.64 mmol) in toluene (140 mL). The resulting mixture was bubbled with nitrogen for 10 minutes then 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (2.97 g, 4.78 mmol) and TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (1.094 g, 1.19 mmol) were added and the mixture was stirred at 110 °C for 20 hours. The reaction mixture was cooled to room temperature then fitered through celite and the filter cake washed with ethyl acetate (500 mL). The filtrate was evaporated to give crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% MeOH in DCM. Pure fractions were evaporated to dryness to afford 1-(4-(benzyloxy)-3-fluorophenyl)piperazine (9.80 g, 71.6 %) as a solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-996b98cdf02a43a3b340c4e4f981f563
Source note750 AstraZeneca ELN dataset