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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191719Generated: November 3, 2026

Cesium carbonate → HCID 68958957, compound

https://huagongshe.com/reaction/2191719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantVinylcyclohexaneHCID 12757—
ReactantTert-butyl 4-bromo-2-(4-fluoroanilino)benzoateHCID 68956988—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
ProductHCID 68958957HCID 68958957—

Reaction Conditions

Temperature110 °C

Reaction Steps

To toluene 3.0 mL solution of tert-butyl 4-bromo-2-(4-fluoroanilino)benzoate 0.20 g were added vinylcyclohexane 0.15 mL, cesium carbonate 0.36 g, tetrabutylammonium bromide 53 mg and polymer-carried bis(acetato)triphenylphosphine palladium(II) 86 mg at room temperature, and it was stirred at 110° C. for 22 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, saturated sodium thiosulfate 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=10:1] to give tert-butyl 4-((E)-2-cyclohexylvinyl)-2-(4-fluoroanilino)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-e957b8011c034a3d9c0a4d91593eb7f1
Source noteuspto-grants-2012_12