Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404292Generated: November 3, 2026

Methyl vinyl ketone → Tert-butyl 9-oxo-3-azaspiro[5.5]undec-7-ene-3-carboxylate

https://huagongshe.com/reaction/2404292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl vinyl ketoneHCID 6570—
ReactantCyclohexaneHCID 8078—
ReactantPotassium HydroxideHCID 14797—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 9-oxo-3-azaspiro[5.5]undec-7-ene-3-carboxylateHCID 59311817—

Reaction Conditions

Temperature-5 °C

Reaction Steps

Methyl vinyl ketone (146 mL) was added to a solution of tert-butyl 4-formylpiperidine-1-carboxylate (375 g) in tetrahydrofuran (18 L). The reaction mixture was cooled to −5° C. and a solution of potassium hydroxide in ethanol (3N, 0.243 L) was added dropwise over 10 minutes. The reaction mixture was allowed to warm to room temperature and stirred for 16 hours. Cyclohexane (10 L) was added and the solution was washed with saturated sodium chloride (3×10 L). The organic layer was concentrated to an oil. This oil was dissolved in 2 L of 80:20 cyclohexane I ethyl acetate and filtered through Celite® to remove insoluble material. The filtrate was purified via flash column chromatography (70:30 hexane I ethyl acetate) to afford the product as an oil. The oil was triturated in hexanes to afford the desired product as a white solid (131 g, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802690B2
Source datasetuspto-grants-2014_08
ORD IDord-2840a25291714125acedec0cd5346021
Source noteuspto-grants-2014_08