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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673458Generated: October 30, 2026

Sodium Carbonate → Tert-butyl 2-(benzamido)-4-(3-chlorophenyl)benzoate

https://huagongshe.com/reaction/1673458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
ReactantTert-butyl 2-(benzamido)-4-bromobenzoateHCID 67343005—
Catalystdicyclohexylphenylphosphine palladium(II)HCID 86634613—
SolventDimethylacetamideHCID 31374—
ProductTert-butyl 2-(benzamido)-4-(3-chlorophenyl)benzoateHCID 67344272—

Reaction Conditions

Temperature90 °C

Reaction Steps

44 mp of 3-chlorophenylboronic 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 90° C. for 15 hours. After the reaction mixture was cooled to room temperature, 5.1 mg of polymer supported di(acetato) dicyclohexylphenylphosphine palladium(II) was added and stirred at 110° C. for 9 hours and 30 minutes. 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 Tribonex Company, eluent; hexane:ethyl acetate=4:1] to obtain tert-butyl 2-(benzamido)-4-(3-chlorophenyl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-4cbafd099ab44f56adacf567cc1c12ba
Source noteuspto-grants-2011_08