HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871878Generated: October 30, 2026
1-Ethylpiperazine → HCID 58748501, compound
https://huagongshe.com/reaction/871878
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Fluoro-2-nitroanisole | HCID 2779250 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58748501 | HCID 58748501 | 77.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975250B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-21d2b592da1e44c8bd082271dee638c2 |
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| Source note | uspto-grants-2015_03 |
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