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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213036Generated: October 31, 2026

1,1-Dimethylethyl 4-(2-propen-1-yl)-4-(2-propen-1-yloxy)-1-piperidinecarboxylate → Tert-butyl 1-oxa-9-azaspiro[5.5]undec-3-ene-9-carboxylate

https://huagongshe.com/reaction/2213036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Dimethylethyl 4-(2-propen-1-yl)-4-(2-propen-1-yloxy)-1-piperidinecarboxylateHCID 21955273—
CatalystBenzylidene-bis(triphenylphosphine)ruthenium dichlorideHCID 60145889—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 1-oxa-9-azaspiro[5.5]undec-3-ene-9-carboxylateHCID 2195528275%

Reaction Steps

Solutions of 1,1-dimethylethyl 4-(2-propenyl)-4-(2-propenyloxy)-1-piperidinecarboxylate (Description 130, 4.9 g, 17.4 mmol) in dichloromethane (1.2 L) and bis(tricyclohexylphosphine)benzylidine ruthenium (IV) dichloride (717 mg, 0.87 mmol) in dichloromethane (1.2 L) were added dropwise simultaneously to dichloromethane (600 mL) over a period of 8 hours, and the mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography on silica gel, eluting with 9:1 isohexane:ethyl acetate, to give the title compound (3.3 g, 75%). m/z (ES+) 254 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105507B2
Source datasetuspto-grants-2006_09
ORD IDord-5aabd353284941e6b687a5ad0c28d942
Source noteuspto-grants-2006_09