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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338671Generated: October 29, 2026

tert-Butanol → Methyl-3-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)benzoate

https://huagongshe.com/reaction/338671

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 3-bromobenzoateHCID 12070—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
SolventTolueneHCID 1140—
ProductMethyl-3-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)benzoateHCID 6005930297.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

Procedure adopted from Tetrahedron Lett., 2007, 48, 2519. A thick-walled glass reaction vessel was charged with palladium(II)acetate (235 mg, 1.05 mmol), X-Phos (500 mg, 1.05 mmol, 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl), cesium carbonate (6.82 g, 20.95 mmol) and 5:1 (v/v) toluene:t-BuOH (20 mL). The stirred contents were purged with nitrogen and a solution of 4-piperidone ethylene ketal (2.70 mL, 20.95 mmol) and methyl-3-bromobenzoate (4.95 g, 23.02 mmol) in 5:1 (v/v) toluene:t-BuOH (100 mL) was added. After stirring for 2 minutes, the vessel was sealed and the reaction mixture was heated at 120° C. for 16 hours. Upon cooling to room temperature, the reaction mixture was filtered through celite and the filtrate was concentrated. Elution through a flash column (silica gel 60, 230-400 mesh, 7:3 hexanes:EtOAc) followed by concentration gave the title compound as an oil (5.64 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889870B2
Source datasetuspto-grants-2014_11
ORD IDord-761c5256799d4ab7bd44e14652109788
Source noteuspto-grants-2014_11