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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant8-Benzyl-2,8-diazaspiro[4.5]decane-1,3-dioneHCID 22110939—
CatalystPalladium hydroxideHCID 9942167—
SolventAcetic AcidHCID 176—
Product2,8-Diazaspiro[4.5]decane-1,3-dioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531546B2
Source datasetuspto-grants-2009_05
ORD IDord-4a08d8d8f86e4608a1d434d3c36cd6ed
Source noteuspto-grants-2009_05