Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4,5-Dichloro-2-nitroaniline | HCID 81149 | — |
| Solvent | Cyclohexanol | HCID 7966 | — |
| Product | HCID 22273264 | HCID 22273264 | 84.9% |
Reaction Steps
Into a solution of 20.02 g of 4,5-dichloro-2-nitroaniline and 8.70 g of piperazine in 100 ml of cyclohexanol, 12.80 g of sodium carbonate was added and stirred at 150° C. for 14 hours. Cooling the reaction liquid to room temperature, water was added and the system was extracted with chloroform. The chloroform layer was dried on anhydrous magnesium sulfate and the solvent was distilled off. Thus obtained residue was washed with diisopropyl ether to provide 21.07 g of 4-chloro-2-nitro-5-(piperazin-1-yl) aniline as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06969712B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-bc7791d27df84f43bfad8bc268e4517b |
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| Source note | uspto-grants-2005_11 |
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