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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673356Generated: October 31, 2026

Cesium carbonate → Tert-butyl 4-(2,4-difluorophenyl)-2-nitrobenzoate

https://huagongshe.com/reaction/1673356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2,4-Difluorophenylboronic acidHCID 2734334—
ReactantTert-butyl 4-chloro-2-nitrobenzoateHCID 63896832—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(2,4-difluorophenyl)-2-nitrobenzoateHCID 6734340348.7%

Reaction Steps

To 15 mL of toluene solution containing 1.5 g of tert-butyl 4-chloro-2-nitrobenzoate, 1.1 g of 2,4-difluorophenylboronic acid, 2.3 g of cesium carbonate, 27 mg of palladium acetate and 25 mg of 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl were added sequentially, and the resulting mixture was heated to reflux under nitrogen atmosphere for 8 hours. After the reaction mixture was cooled to room temperature, insoluble were removed by filtration and added a saturated sodium hydrogen carbonate aqueous solution. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with 10% citric acid aqueous solution and a saturated sodium chloride aqueous solution sequentially, and the solvent was evaporated under reduced pressure. Hexane and diisopropyl ether were added to the obtained residue and a solid substance was separated by filtration to obtain 0.95 g of tert-butyl 4-(2,4-difluorophenyl)-2-nitrobenzoate as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-f1b22ebecb064c74a735385689c4eec3
Source noteuspto-grants-2011_08