HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370604Generated: October 31, 2026
Hydrochloric Acid → 5,7-diazaspiro[3.4]octane-6,8-dione
https://huagongshe.com/reaction/2370604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Reactant | Water ethanol | HCID 19096565 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,7-diazaspiro[3.4]octane-6,8-dione | HCID 242823 | 39% |
Reaction Steps
Sodium cyanide (1.47 g, 30 mmole) then ammonium carbonate (7.5 g, 78 mmole) are added under argon and at 23° to a solution of cyclobutanone (1.49 ml, 20 mmole) diluted in an ethanol-water solvent mixture (16 ml). The reaction mixture is heated for 6 hours at 70° C. After cooling down the reaction medium, water (15 ml) is poured in, then a solution of concentrated hydrochloric acid (13 ml) is added carefully. After stirring for 10 hours at 23° C. the ethanol and part of the water content of the reaction mixture are evaporated with a rotary evaporator. The precipitate is filtered on frit then washed with water. The expected compound is obtained in the form of a beige powder with a yield of 39% (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710091B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-d5e38befd5154571b75d4c1bf43ee6ce |
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| Source note | uspto-grants-2014_04 |
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