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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191852Generated: November 1, 2026

Cesium carbonate → HCID 68958760, compound

https://huagongshe.com/reaction/2191852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantN-(3-Bromophenyl)acetamideHCID 12123—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantTert-butyl 3-amino-[1,1'-biphenyl]-4-carboxylateHCID 58508425—
Catalystpalladium(II) acetateHCID 167845—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
ProductHCID 68958760HCID 68958760—

Reaction Conditions

Temperature80 °C

Reaction Steps

To 2-methyl-2-propanol 2.5 mL solution of tert-butyl 2-amino-4-phenylbenzoate 0.12 g were added cesium carbonate 0.29 g, N-(3-bromophenyl)acetamide 0.14 g, 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl 11 mg, tris(dibenzylideneacetone)dipalladium(0) 4.0 mg and palladium acetate 2.0 mg at room temperature, and it was stirred at 80° C. for 4 hours. Tris(dibenzylideneacetone)dipalladium(0) 4.0 mg, palladium acetate 2.0 mg and 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl 11 mg were added to it at room temperature, and it was stirred at 80° C. for 12 hours. After the reaction mixture was cooled to room temperature, ethyl acetate and water were added to it. The organic layer was separated and collected,dried over anhydrous magnesium sulfate after washing with saturated sodium chloride aqueous solution, and the solvent was removed under reduced pressure. The obtained residue was refined by silica gel column chromatography [Trikonex company, Flash Tube 2008, eluent; hexane:ethyl acetate=2:1] to give tert-butyl 2-((3-(acetamido)phenyl)amino)-4-phenylbenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-467604ca8aed44aa863a9abcf4321016
Source noteuspto-grants-2012_12