Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888994Generated: October 26, 2026

Triethyloxonium tetrafluoroborate → 1-[(2-Chlorophenyl)carbonyl]-3-(ethyloxy)piperazine

https://huagongshe.com/reaction/1888994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactant4-[(2-Chlorophenyl)carbonyl]-2-piperazinoneHCID 31095825—
SolventDichloromethaneHCID 6344—
Product1-[(2-Chlorophenyl)carbonyl]-3-(ethyloxy)piperazineHCID 67533358—

Reaction Conditions

Temperature25 °C

Reaction Steps

4-[(2-chlorophenyl)carbonyl]-2-piperazinone (I4) (676 mg, 2.83 mmol) was dissolved in dichloromethane (DCM) (10 mL) and was treated with triethyloxonium tetrafluoroborate (628 mg, 3.31 mmol). The solution was stirred at 25° C. for 16 hr and the solution partitioned between ethyl acetate (25 mL) and saturated sodium bicarbonate solution (25 mL). The aqueous phase was extracted with ethyl acetate (3×25 mL), combined extracts were washed with brine (25 mL), dried over anhydrous sodium sulfate and concentrated to a crude oil in 816 mg that was used in the subsequent step without further purification. Compound was not characterised but used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501946B2
Source datasetuspto-grants-2013_08
ORD IDord-14bb6c053b484a4e90b40085625e7b2a
Source noteuspto-grants-2013_08