Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71Generated: October 24, 2026

1-Acetylpiperazine → 1-[4-(2-Methyl-3-nitrophenyl)piperazin-1-yl]ethanone

https://huagongshe.com/en/reaction/71

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AcetylpiperazineHCID 83795—
Reactant2-Bromo-6-nitrotolueneHCID 123537—
ReagentCesium carbonateHCID 10796—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystPalladium (II) acetateHCID 4144353—
SolventTolueneHCID 1140—
Product1-[4-(2-Methyl-3-nitrophenyl)piperazin-1-yl]ethanoneHCID 6859297798.46%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-bromo-2-methyl-3-nitrobenzene (500 mg, 2.31 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (201 mg, 0.35 mmol) and cesium carbonate (1131 mg, 3.47 mmol) and diacetoxypalladium (52.0 mg, 0.23 mmol) were dissolved in toluene (10 mL) and sealed into a microwave tube degazed and purged with argon. The reaction was heated to 100 °C, over a period of 12 hours. The reaction mixture was cooled down to room temperature, filtered and the residue was evaporated. The crude product was purified by flash chromatography on silica gel eluting with 0 to 10% methanol in dichloromethane. The solvent was evaporated to dryness to afford 1-(4-(2-methyl-3-nitrophenyl)piperazin-1-yl)ethanone (600 mg, 98 %) as a solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-57be3c43ca2f40d482cab5a1bd42b5d5
Source note750 AstraZeneca ELN dataset