HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → tert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hydroxylamine HCl | HCID 21645 | — |
| Reactant | tert-Butyl 4-cyanopiperazine-1-carboxylate | HCID 14068968 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylate | HCID 178452346 | 86.4% |
Reaction Steps
In a nitrogen atmosphere, a suspension of 7.52 g of tert-butyl 4-cyanopiperazine-1-carboxylate (JMC, 1988, 31, 1036), 7.46 g of hydroxyammonium chloride and 19.7 g of potassium carbonate in 40 ml of ethanol was heated to reflux for 2 hours. The residue prepared by evaporation of the solvent was diluted with ethyl acetate, washed with water and then with a saturated saline solution and dried over sodium sulfate. The solvent was evaporated in vacuo to give 7.51 g of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858800B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-7907d2e4b2ce4cc387d562b55774d64c |
| Source note | uspto-grants-2010_12 |