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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051982Generated: October 30, 2026

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

https://huagongshe.com/reaction/1051982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantMethyl 3-bromobenzoateHCID 12070—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Solventtert-ButanolHCID 6386—
ProductMethyl-3-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)benzoateHCID 60059302—

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388176B2
Source datasetuspto-grants-2016_07
ORD IDord-d3973b10688b4c2a97a5e2ce273c5f9b
Source noteuspto-grants-2016_07