HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586770Generated: October 30, 2026
Potassium Carbonate → tert-Butyl 4-(2-methyl-4-nitrophenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/586770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, 1-fluoro-2-methyl-4-nitro- | HCID 68001 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl 4-(2-methyl-4-nitrophenyl)piperazine-1-carboxylate | HCID 22336105 | 62% |
Reaction Steps
4.65 g (3.10 mmol) of 2-fluoro-5-nitrotoluene, 6.71 g (3.60 mmol) of tert-butyl 1-piperazinecarboxylate and 10.4 g (7.50 mmol) of potassium carbonate are solubilized under an argon atmosphere, in dry DMF (50 ml), then the reaction medium is taken to 80° C. for 18 hours. The reaction medium is then cooled down using an ice bath then poured into ice-cold water. The product is extracted using 3 times 50 ml of ethyl acetate. The organic solution is dried over magnesium sulphate, followed by filtration and concentration under vacuum. Purification is then carried out by crystallization from diisopropyl ether and the solid obtained is filtered and rinsed with isopentane in order to obtain, after drying, 5.9 g of a yellow solid product (yield 62%). Melting point: 121.8-123.4° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936715B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-6b658cff99964004beade35b7bebd8f3 |
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| Source note | uspto-grants-2005_08 |
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