HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557710Generated: October 31, 2026
Potassium Carbonate → tert-Butyl 4-(2-cyano-4-nitrophenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/557710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 2-Fluoro-5-nitrobenzonitrile | HCID 519417 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 4-(2-cyano-4-nitrophenyl)piperazine-1-carboxylate | HCID 22227995 | 59.2% |
Reaction Steps
A solution of 2-fluoro-5-nitrobenzonitrile (500 mg, 3.0 mmol) in ethanol (35 mL) was treated with potassium carbonate (420 mg, 3.0 mmol) and piperazine-1-carboxylic acid tert-butyl ester (560 mg, 3.0 mmol). The reaction mixture was stirred at 80° C. for 1 h, then cooled and partitioned between ethyl acetate and water. The organic layer was then collected, dried over sodium sulfate, filtered and evaporated to a yellow residue. Purification using flash chromatography yielded 4-(2-cyano-4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (590 mg, 59% yield) as a bright yellow solid. HRMS calcd for C16H20N4O4 (M+Na) 355.1377, obsd 355.1376.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058299B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-71c2aaa4cc3a4854957e87ed703648d6 |
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| Source note | uspto-grants-2011_11 |
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