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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673378Generated: October 31, 2026

Citric Acid → HCID 57879555, compound

https://huagongshe.com/reaction/1673378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantCesium carbonateHCID 10796—
ReactantVinylcyclohexaneHCID 12757—
ReactantTert-butyl 2-(benzamido)-4-bromobenzoateHCID 67343005—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 57879555HCID 57879555—

Reaction Conditions

Temperature110 °C

Reaction Steps

0.037 mL of vinylcyclohexane, 87 mg of cesium carbonate, 13 mg of tetrabutylammonium bromide and 21 mg of polymer supported di(acetato)dicyclohexylphosphino palladium(11) were added to 1.0 mL of toluene solution containing 50 mg of tert-butyl 2-(benzamido)-4-bromobenzoate at room temperature and stirred at 110° C. for 48 hours. After the reaction mixture was cooled to room temperature, ethyl acetate and 10% citric acid aqueous solution were added. The organic layer was separated, and the solvent was evaporated under reduced pressure after washed with 10% citric acid aqueous solution. 5 mL of trifluoroacetic acid; was added to the obtained residue and stirred at room temperature for 1 hour. The solvent was evaporated under reduced pressure, and the obtained residue was purified with reversed-phase silica gel column chromatography [eluent; 55-100% acetonitrile/0.1% trifluoroacetic acid aqueous solution] to obtain 2.9 mg of 2-(benzamido)-4-((E)-2-cyclohexylvinyl)benzoic acid as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-664cee59ba464bdea5cab9255267215b
Source noteuspto-grants-2011_08