HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491463Generated: October 30, 2026
Ethanol → 2,8-Diazaspiro[4.5]decane-1,3-dione
https://huagongshe.com/reaction/491463
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | 8-Benzyl-2,8-diazaspiro[4.5]decane-1,3-dione | HCID 22110939 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2,8-Diazaspiro[4.5]decane-1,3-dione | HCID 15671041 | — |
Reaction Steps
To 8-benzyl-2,8-diaza-spiro[4.5]decane-1,3-dione (28.3 g, 0.11 mol) and Pd(OH)2 (8.5 g) in 2 l of flask, EtOH (438 ml) and acetic acid (5.5 ml) are added at ambient temperature. The reaction mixture is stirred under H2 at room temperature for 15 h. The catalysts are removed by filtration and EtOH is evaporated down to give 2,8-diaza-spiro[4.5]decane-1,3-dione in quantitative yield. To a suspension of 2,8-diaza-spiro[4.5]decane-1,3-dione (4.2 g, 25.2 mmol) in dichloromethane (60 ml), 1N NaOH (26 ml, 26 mmol) and di-t-butyldicarbonate (6.1 g, 27.7 mmol) in dichloromethane (20 ml) are added at ambient temperature. The reaction mixture is stirred for 15 h. 10% Citric acid is added to the reaction mixture and the pH of the mixture is adjusted to 5. The combined extracts are washed with brine, dried over magnesium sulfate and concentrated under vacuum to give solid product, which filtrated with diethyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531546B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-4a08d8d8f86e4608a1d434d3c36cd6ed |
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| Source note | uspto-grants-2009_05 |
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