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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191768Generated: November 3, 2026

Toluene → Tert-butyl 4-(4-(dimethylamino)phenyl)-2-(4-fluoroanilino)benzoate

https://huagongshe.com/reaction/2191768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Dimethylamino)phenylboronic acidHCID 2734344—
ReactantTert-butyl 4-bromo-2-(4-fluoroanilino)benzoateHCID 68956988—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(4-(dimethylamino)phenyl)-2-(4-fluoroanilino)benzoateHCID 68965065—

Reaction Steps

To toluene 1.6 mL solution of tert-butyl 4-bromo-2-(4-fluoroanilino)benzoate 70 mg were added ethanol 0.60 mL, water 0.30 mL, 4-(dimethylamino)phenylboronic acid 47 mg, sodium hydrogen carbonate 48 mg and tetrakis(triphenylphosphine)palladium(0) 11 mg at room temperature, and it was heated and refluxed for 6 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 [Fuji SILYSIA Chemical Ltd., PSQ100B(spherical type), eluent; hexane:ethyl acetate=10:1] to give tert-butyl 4-(4-(dimethylamino)phenyl)-2-(4-fluoroanilino)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-fba4b05860464168ae93855018b92540
Source noteuspto-grants-2012_12