HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605972Generated: October 27, 2026
p-Fluoronitrobenzene → 1-Tert-butyl-4-(4-nitrophenyl)piperazine
https://huagongshe.com/reaction/605972
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Tert-butylpiperazine | HCID 3530572 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ammonia | HCID 222 | — |
| Product | 1-Tert-butyl-4-(4-nitrophenyl)piperazine | HCID 57444158 | 118.5% |
Reaction Steps
To a solution of 1-fluoro-4-nitro-benzene (314 mg, 2.23 mmol) and 4-tert-butyl-piperazine (1 g, 3.34 mmol) in dioxane (15 mL) is added K2CO3 (1.65 mg, 11.9 mmol) and the reaction is stirred at 130° C. overnight. The solvent is evaporated under vacuum and the residue is partitioned between ethyl acetate and water. The organic layer is washed with brine, dried over MgSO4, filtered and concentrated to give a crude compound. Purification by silica gel column chromatography eluting with DCM followed by 99:1 DCM:NH3 (7M in MeOH) affords the title compound (348 mg, 55.4%). LCMS: Rt 3.87 min (99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07915256B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-577d6d26b4564c8a92062e309778b44a |
|---|
| Source note | uspto-grants-2011_03 |
|---|