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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871878Generated: October 30, 2026

1-Ethylpiperazine → HCID 58748501, compound

https://huagongshe.com/reaction/871878

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-EthylpiperazineHCID 79196—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Fluoro-2-nitroanisoleHCID 2779250—
SolventAcetonitrileHCID 6342—
ProductHCID 58748501HCID 5874850177.3%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 3.42 g (20 mmol) of 4-fluoro-2-methoxy-1-nitrobenzene, 2.67 mL (21 mmol) of 1-ethylpiperazine and 5.14 mL (30 mmol) of diisopropylethylamine in 25 mL of acetonitrile is heated for 2.5 hours at 85°C. and then for 1 hour at 95°C., and is then stirred overnight while allowing to return to room temperature. The acetonitrile is evaporated off and the residue is then taken up in 50 mL of ether and 25 mL of water. The aqueous phase is extracted with ether. The organic phases are combined, dried over Na2SO4, filtered and concentrated under vacuum. The oil obtained is triturated in an ether/cyclohexane mixture (1/1) and the precipitate is isolated by filtration, rinsed with pentane and dried in an oven. 4.1 g of the expected product are finally obtained. Yield=77%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975250B2
Source datasetuspto-grants-2015_03
ORD IDord-21d2b592da1e44c8bd082271dee638c2
Source noteuspto-grants-2015_03