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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569Generated: October 23, 2026

Bromobenzene → 1,2-Diphenylpiperidine

https://huagongshe.com/en/reaction/569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
Reactant2-PhenylpiperidineHCID 103020—
ReagentCesium carbonateHCID 10796—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
Solvent1,4-DioxaneHCID 31275—
Product1,2-DiphenylpiperidineHCID 1243476415.56%

Reaction Conditions

Temperature100 °C

Reaction Steps

Caesium carbonate (556 mg, 1.71 mmol) was added to bromobenzene (0.060 mL, 0.57 mmol) and 2-phenylpiperidine (110 mg, 0.68 mmol) in 1,4-dioxane (2 mL). The reaction was degassed and Tris(dibenzylideneacetone)?dipalladium(0) (13.01 mg, 0.01 mmol) and dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine (RuPhos) (13.26 mg, 0.03 mmol) were added. The resulting solution was stirred at 100 °C for 16 hours. LCMS showed The reaction mixture was diluted with EtOAc, and washed with water. The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 15% MeOH in DCM. Pure fractions were evaporated to dryness to afford 1,2-diphenylpiperidine (21.00 mg, 15.56 %) as a yellow oil. f0 = 19 mg bromobenzene f1 = 21 mg product The reaction was abandonned.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-bd4700a79525457dbcfd3c5e1368118f
Source note750 AstraZeneca ELN dataset