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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274971Generated: October 30, 2026

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

https://huagongshe.com/reaction/2274971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantMethyl vinyl ketoneHCID 6570—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantBenzyl 4-formylpiperidine-1-carboxylateHCID 2776272—
ProductBenzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylateHCID 2343573257.2%

Reaction Steps

Benzyl 4-formylpiperidine-1-carboxylate (5.17 g, 20.907 mmol) and p-Toluenesulfonic acid monohydrate (0.398 g, 2.091 mmol) were stirred in Benzene (30.0 ml, 334.136 mmol) at 70° C. But-3-en-2-one (3.76 ml, 41.813 mmol) was added and the reaction mixture was refluxed o/n while removing water with dean-stark trap. After cooling the reaction mixture to rt, sat. NaHCO3 soln. was added and the organic layer was dried over Na2SO4 and evaporated. The resulting oil was purified by Biotage (SiO2, 250 g, EtOAc/Hep 10% to 50%) to afford the title compound (3.58 g, 11.96 mmol, 57.2% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126999B2
Source datasetuspto-grants-2015_09
ORD IDord-24173da873b440488f373cb24b05c467
Source noteuspto-grants-2015_09