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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191727Generated: November 3, 2026

Cesium carbonate → HCID 68960663, compound

https://huagongshe.com/reaction/2191727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBenzene, 1-iodo-3-methoxy-HCID 69839—
ReactantTert-butyl 2-(4-fluoroanilino)-4-vinylbenzoateHCID 68959213—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
ProductHCID 68960663HCID 68960663—

Reaction Conditions

Temperature110 °C

Reaction Steps

To toluene 3.0 mL solution of tert-butyl 2-(4-fluoroanilino)-4-vinylbenzoate 0.12 g were added 3-iodoanisole 0.18 g, cesium carbonate 0.25 g, tetrabutylammonium bromide 37 mg and polymer-carried bis(acetato)triphenylphosphine palladium(II) 58 mg at room temperature, and it was stirred at 110° C. for 24 hours. After the reaction mixture was cooled to room temperature, insoluble matter was filtrated, ethyl acetate and 10% citric acid aqueous solution were added to it. The organic layer was separated and collected, dried over anhydrous magnesium sulfate after sequential washing with 10% citric acid aqueous solution and 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=4:1] to give tert-butyl 2-(4-fluoroanilino)-4-((E)-2-(3-methoxyphenyl)vinyl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-93d0d9abfcad418a86e56870ca0e4f17
Source noteuspto-grants-2012_12