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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181933Generated: November 1, 2026

Cesium carbonate → 1-(5-Tert-butyl-2-methoxy-3-nitro-phenyl)-azetidin-2-one

https://huagongshe.com/reaction/1181933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-AzetidinoneHCID 136721—
Reactant1-Bromo-5-(tert-butyl)-2-methoxy-3-nitrobenzeneHCID 57550024—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product1-(5-Tert-butyl-2-methoxy-3-nitro-phenyl)-azetidin-2-oneHCID 57550023106.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

An oven-dried Schlenk tube was charged with the above nitroanisole (500 mg, 1.74 mmol), 2-azetidinone (150 mg, 2.1 mmol), tris(dibenzylideneacetone)dipalladium(0) (32 mg, 0.035 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (58 mg, 0.1 mmol) and cesium carbonate (795 mg, 2.44 mmol). The tube was capped with a rubber septum, purged with argon and 1,4-dioxane (7 mL) was then added through the septum via a syringe. The tube was sealed with a teflon screwcap and the reaction mixture was stirred at 100° C. for 20 h. The reaction mixture was cooled to room temperature, diluted with EtOAc (100 mL), washed with water, brine and dried over anhydrous Na2SO4. The solvent was removed in vacuo, and the crude product was purified by column chromatography (2:1 hexane-EtOAc) to give 1-(5-tert-butyl-2-methoxy-3-nitro-phenyl)-azetidin-2-one (516 mg, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285545B2
Source datasetuspto-grants-2007_10
ORD IDord-23afa50e6cbd4b979c2c394a0b72534a
Source noteuspto-grants-2007_10