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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531034Generated: October 30, 2026

Sodium Carbonate → Ethyl 5-cyclopropyl-2-ethoxy-6-(4-fluorophenyl)nicotinate

https://huagongshe.com/reaction/531034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantEthyl 5-bromo-2-ethoxy-6-(4-fluorophenyl)nicotinateHCID 90424072—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductEthyl 5-cyclopropyl-2-ethoxy-6-(4-fluorophenyl)nicotinateHCID 11799247196%

Reaction Steps

Tris(dibenzylideneacetone)dipalladium(0) (418 mg) was added to a mixture of ethyl 5-bromo-2-ethoxy-6-(4-fluorophenyl)nicotinate (2.40 g), cyclopropylboronic acid (1.68 g), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (401 mg), a 2 M aqueous sodium carbonate solution (9.78 mL), and toluene (25 mL), and the resultant mixture was stirred at 100° C. for 2 hours in an argon atmosphere. The reaction mixture was allowed to cool to room temperature and poured to water, followed by extraction with ethyl acetate. The obtained organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (2.06 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353108B2
Source datasetuspto-grants-2016_05
ORD IDord-1c09d0dcb3014bd386e575f6feca73a9
Source noteuspto-grants-2016_05