HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509088Generated: October 27, 2026
Water → Tert-butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/509088
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 5-Fluoro-2-nitroaniline | HCID 75399 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylate | HCID 22272542 | 82% |
Reaction Steps
To a solution of 5-fluoro-2-nitroaniline (10 g, 64.1 mmol) in DMF (65 mL) was added tert-butyl-piperazine carboxylate (13.1 g, 70.5 mmol) and K3PO4 (13.3 g, 96.2 mmol). The reaction mixture was stirred at 100° C. overnight. After adding 100 ml H2O into the solution, the precipitated yellow solid was filtered under vacuum then dried in vacuo to afford tert-butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylate as yellow solid (15 g, yield: 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096549B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-19c1eeebeab942babdd98ab1ccdfcac2 |
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| Source note | uspto-grants-2015_08 |
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