HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496962Generated: October 25, 2026
1,3-Dinitrobenzene → Tert-butyl 4-(3-fluoro-4-nitrophenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1496962
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dinitrobenzene | HCID 7452 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | tert-Butyl 4-(5-Fluoro-2-nitrophenyl)piperazine-1-carboxylate | HCID 22272537 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 4-(3-fluoro-4-nitrophenyl)piperazine-1-carboxylate | HCID 66738172 | — |
Reaction Steps
2,4-dinitrobenzene (1.2 g), N-Boc-piperazine (1.4 g) and potassium carbonate (1.2 g) were dissolved in dimethylformamide (5 mL) and stirred at 50° C. overnight. Then, the mixture was distilled under reduced pressure to remove dimethylformamide, added with water, and extracted with ethyl acetate. The thus obtained organic layer was washed with brine, and water was removed with sodium sulfate, and the solvent was removed by distillation under reduced pressure. The mixture was purified by column chromatography (silica gel) to obtain target compounds (Rf=0.3, hexane:ethyl acetate=2:1) and (tert-butyl-4-(5-fluoro-2-nitrophenyl)piperazin-1-carboxylate (Rf=0.6, hexane:ethyl acetate=2:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199944B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-33434855225a4960ab79bee64b09fab3 |
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| Source note | uspto-grants-2015_12 |
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