HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705721Generated: October 29, 2026
Potassium Carbonate → Tert-butyl 4-(3-methoxy-4-nitrophenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/705721
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 5-Fluoro-2-nitroanisole | HCID 2779250 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl 4-(3-methoxy-4-nitrophenyl)piperazine-1-carboxylate | HCID 25918710 | 66.9% |
Reaction Steps
A mixture of 5-fluoro-2-nitroanisole (3.00 g, 17.5 mmol), tert-butyl piperazine-1-carboxylate (4.57 g, 24.5 mmol) and potassium carbonate (3.63 g, 26.3 mmol), in dimethyl sulfoxide (20 mL) was heated at 90° C. for 1.5 hours under a nitrogen atmosphere. The reaction mixture was cooled and diluted with water (100 mL). The resulting precipitate was filtered and dried to give a bright yellow solid. The solid was suspended in a 5:1 solution of petroleum ether/diethyl ether (50 mL), sonicated for 2 minutes, filtered and dried to give the title compound (I1) (3.95 g, 66%) as a bright yellow solid; 1H NMR (300 MHz, d6-DMSO) δ 1.42 (s, 9H), 3.46 (brs, 8H), 3.90 (s, 3H), 6.52 (s, 1H), 6.57 (d, 1H, J=9.5 Hz) and 7.89 (d, 1H, J=9.3 Hz). LCMS Method B: rt 7.45 min; m/z 338.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174946B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-6fee18d7ca914542af16952ede56d693 |
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| Source note | uspto-grants-2015_11 |
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