Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453909Generated: October 27, 2026

Water → Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylate

https://huagongshe.com/reaction/453909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl vinyl ketoneHCID 6570—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzyl 4-formylpiperidine-1-carboxylateHCID 2776272—
SolventEthanolHCID 702—
ProductBenzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylateHCID 23435732—

Reaction Steps

Methyl vinyl ketone (1.64 ml), ethanol (5 ml) and water (5 ml) were added to benzyl 4-formylpiperidine-1-carboxylate (5 g). The mixture was then added to a boiling solution of potassium hydroxide (0.22 g) in ethanol (10 ml), and the resulting reaction mixture was refluxed for 1 h (TLC monitoring). When the reaction was complete, the mixture was added to water (25 ml) and extracted with ethyl acetate (2×50 ml). The combined organic phases were dried (Na2SO4) and concentrated under vacuum. The crude product so obtained was purified by column chromatography (silical gel, 25% ethyl acetate/hexane). Yield: 2.8 g (46%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492559B2
Source datasetuspto-grants-2013_07
ORD IDord-7fd02a2c35ef4e0eac9004362790dfbc
Source noteuspto-grants-2013_07