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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673462Generated: November 4, 2026

Sodium Carbonate → Tert-butyl 2-(benzamido)-4-(4-phenoxyphenyl)benzoate

https://huagongshe.com/reaction/1673462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
ReactantTert-butyl 2-(benzamido)-4-bromobenzoateHCID 67343005—
Catalystdicyclohexylphenylphosphine palladium(II)HCID 86634613—
SolventDimethylacetamideHCID 31374—
ProductTert-butyl 2-(benzamido)-4-(4-phenoxyphenyl)benzoateHCID 67341966—

Reaction Conditions

Temperature110 °C

Reaction Steps

60 mg of 4-phenoxyphenylboronic acid, 49 mg of sodium carbonate and 6 mg of polymer supported di(acetato) dicyclohexylphenylphosphine palladium(II) were added to 2.5 mL of N,N-dimethylacetamide solution containing 70 mg of tert-butyl 2-(benzamido)-4-bromobenzoate, and stirred at: 110° C. for 24 hours. After the reaction mixture was cooled to room temperature, 6 mg of polymer supported di(acetato) dicyclohexylphenylphosphine palladium(II) was added and stirred at 110° C. for 24 hours. After the reaction mixture was cooled to room temperature, insoluble were removed by filtration and ethyl acetate and 10% citric acid aqueous solution were added. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with 10% citric acid aqueous solution and a saturated sodium chloride aqueous solution sequentially, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [Flash Tube 2008 manufactured by Trikonex company, eluent; hexane: ethyl acetate=4:1] to obtain tert-butyl 2-(benzamido)-4-(4-phenoxyphenyl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-a411bd86c0a241468335082f2f11aead
Source noteuspto-grants-2011_08