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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501760Generated: October 27, 2026

Water → Tert-butyl 1-oxo-2-(5-oxo-2,5-dihydrofuran-3-yl)-2,8-diazaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/1501760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant4-bromo-5H-furan-2-oneHCID 11789536—
Reactanttert-Butyl 1-oxo-2,8-diazaspiro[4.5]decane-8-carboxylateHCID 45073946—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductTert-butyl 1-oxo-2-(5-oxo-2,5-dihydrofuran-3-yl)-2,8-diazaspiro[4.5]decane-8-carboxylateHCID 86709449—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of tert-butyl 1-oxo-2,8-diazaspiro[4.5]decane-8-carboxylate (1.83 g, 7.20 mmol), commercially available 4-bromofuran-2(5H)-one (1.41 g, 8.63 mmol), Xantphos (0.416 g, 0.720 mmol), water (0.389 mL, 21.6 mmol), and potassium carbonate (1.989 g, 14.39 mmol) in toluene (50 mL) was degassed with nitrogen followed by addition of palladium acetate (0.081 g, 0.36 mmol). The resulting mixture was heated at 65° C. for 16 h. After filtration through CELITE®, the filtrate was concentrated and the residue was purified on silica gel column using EtOAc /hexane as eluting solvents to give the title compound. LC/MS: (M+1)+: 337.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206198B2
Source datasetuspto-grants-2015_12
ORD IDord-9a30b6ef169e4d889984c4c6c55ff2af
Source noteuspto-grants-2015_12