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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036085Generated: October 30, 2026

Water → Benzyl 1-oxa-5-azaspiro(2.5)octane-5-carboxylate

https://huagongshe.com/reaction/2036085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactant1-Benzyloxycarbonyl-3-piperidoneHCID 1514169—
SolventDimethyl SulfoxideHCID 679—
ProductBenzyl 1-oxa-5-azaspiro(2.5)octane-5-carboxylateHCID 7164949760%

Reaction Steps

To a solution of trimethylsulfoxonium iodide (3.1 g) in dimethyl sulfoxide (40 mL) was added sodium hydride (570 mg), and the mixture was stirred at room temperature for 1 hr. A solution of benzyl 3-oxopiperidine-1-carboxylate (3.0 g) in dimethyl sulfoxide (10 mL) was added under ice-cooling, and the mixture was stirred at room temperature for 16 hr. To the reaction solution was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over sodium sulfate and concentrated. The residue was purified by silica gel column chromatography (30% ethyl acetate/hexane to 50% ethyl acetate/hexane) to give the object product (1.9 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575167B2
Source datasetuspto-grants-2013_11
ORD IDord-d96b08410ce44f62a0cf936a36773211
Source noteuspto-grants-2013_11