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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Reactant | 4-[(2-Chlorophenyl)carbonyl]-2-piperazinone | HCID 31095825 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[(2-Chlorophenyl)carbonyl]-3-(ethyloxy)piperazine | HCID 67533358 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501946B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-14bb6c053b484a4e90b40085625e7b2a |
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| Source note | uspto-grants-2013_08 |
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