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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253716Generated: November 2, 2026

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

https://huagongshe.com/reaction/1253716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl vinyl ketoneHCID 6570—
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 5931181725%

Reaction Conditions

Temperature25 °C

Reaction Steps

3 N KOH in ethanol (7.5 ml) was added to mixture of tert-butyl 4-formylpiperidine-1-carboxylate (60.0 mmol, 1.0 eq.) and methyl vinyl ketone (70.0 mmol, 1.3 eq.) in THF (100 ml) at 0° C. and the mixture was then stirred at 25° C. for 16 h. The solvent was evaporated under reduced pressure and the residue diluted with water (100 ml) and KHSO4 solution at 0° C. The aqueous layer was extracted with MC (2×150 ml). The combined organic layers were washed with brine (100 ml) and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the crude product was purified by silica gel column chromatography eluting with 10-12% ethyl acetate in hexanes to give the desired product as a light brown sticky solid. Yield: 25%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455475B2
Source datasetuspto-grants-2013_06
ORD IDord-23a2e45b535147b0aaaf324cc8c6e981
Source noteuspto-grants-2013_06