HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922816Generated: October 26, 2026
Ethanol → 1,3-Diazaspiro(4.7)dodecane-2,4-dione
https://huagongshe.com/reaction/922816
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Cyclooctanone | HCID 10403 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Diazaspiro(4.7)dodecane-2,4-dione | HCID 95195 | 73% |
Reaction Steps
To a mixture of cyclooctanone (GA, 17 g, 135 mmol, Sigma-Aldrich) in ethanol (200 mL) and water (200 mL) were added KCN (17.5 g, 269 mmol, Sigma-Aldrich) followed by ammonium carbonate ([NH4]2CO3, 51.8 g, 539 mmol, Sigma-Aldrich). The resulting reaction mixture was stirred at 80° C. for 6 h. The reaction mixture was evaporated to dryness under reduced pressure to provide a white solid precipitate which was filtered, collected, and dried for 16 h to provide 15.9 g of the compound of formula GB, 1,3-diazaspiro[4.7]dodecane-2,4-dione (yield 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09278967B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-e2bd9552d70c421b845d29e4c5bbddd5 |
|---|
| Source note | uspto-grants-2016_03 |
|---|