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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596672Generated: October 30, 2026

Methyl vinyl ketone → Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylate

https://huagongshe.com/reaction/1596672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl vinyl ketoneHCID 6570—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzyl 4-formylpiperidine-1-carboxylateHCID 2776272—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductBenzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylateHCID 23435732—

Reaction Steps

A solution of 0.98 g (3.96 mmol) benzyl 4-formylpiperidine-1-carboxylate (prepared by the method from Eur. J. Med. Chem. 1991, 26, 625) and 0.28 g (4.0 mmol) 3-buten-2-one in a mixture of 1 ml methanol and 1 ml water was added dropwise to a boiling solution of 0.015 g (0.27 mmol) potassium hydroxide in 1 ml methanol. After 1 hour heating with reflux the cooled mixture was poured into 50 ml water, and it was extracted with tert.-butylmethylether. The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The title compound was obtained from the remaining oil by HPLC on silica gel with hexane/acetone 4:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291469B1
Source datasetuspto-grants-2001_09
ORD IDord-401fd82f3fdc449c88a395ddb82d9e92
Source noteuspto-grants-2001_09