HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940167Generated: October 31, 2026
Water → N-tert-Butylpiperazine-2-carboxamide
https://huagongshe.com/reaction/1940167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21466124 | HCID 21466124 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | N-tert-Butylpiperazine-2-carboxamide | HCID 11008617 | 55% |
Reaction Steps
In 1029 g (8.40 moles) of an aqueous 80% sulfuric acid was dissolved 219.5 g (1.05 mole) of 2-cyanopiperazine sulfate with stirring while keeping the temperature below 40° C. Then, while maintaining the temperature of from 9° C. to 15° C., to the solution was added dropwise 187 g (2.52 moles) of tert-butyl alcohol over a period of 3 hours and further, the mixture was kept at the same temperature for 2.5 hours to complete the reaction. Then, after adding 3 liters of water to the reaction liquid thus obtained, the mixture was neutralized with an aqueous solution of 25% sodium hydroxide until pH thereof became 10. Then, the reaction liquid was extracted twice with one liter of chloroform, the extracts were combined with each other, and chloroform was removed from the mixed extract under reduced pressure to provide 106.8 g (yield 55%) of N-tert-butyl-2-piperazine carboxamide having a melting point of from 151° C. to 152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05698697 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-9c1fe2d02df64669a79c2855d3db0443 |
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| Source note | uspto-grants-1997_12 |
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