Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14833063 | HCID 14833063 | — |
Reaction Steps
All operations are carried out under a blanket of N2. 1 mol of each of NaHCO3 and piperidine are introduced into 0.8 1 of water, and 0.5 mol of cyanuric chloride is added in portions at room temperature sufficiently slowly that the reaction temperature is 20° C. and the pH is between 7 and 11. The reaction mixture is subsequently stirred at 20° C. for a further 100 minutes and refluxed for 30 minutes. After cooling, 0.25 mol of each of piperazine and Na2CO3 as 13% strength by weight and 20% strength by weight aqueous solutions respectively are added simultaneously, and the mixture is stirred at room temperature for a further 2 hours and refluxed for 17 hours. The resultant suspension is filtered with suction, washed with water and the residue is dried to constant weight. A finely crystalline, white powder is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05099017 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-163097b72aa341b7a97c9f1ff0fde0a5 |
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| Source note | uspto-grants-1992_03 |
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