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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709762Generated: October 29, 2026

Sodium Carbonate → Methyl 6-(2-fluoro-5-methoxyphenyl)-5-isobutoxynicotinate

https://huagongshe.com/reaction/709762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Fluoro-5-methoxyphenylboronic acidHCID 4157211—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantMethyl 6-chloro-5-isobutoxynicotinateHCID 117760029—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductMethyl 6-(2-fluoro-5-methoxyphenyl)-5-isobutoxynicotinateHCID 11776030372.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

Under an argon atmosphere, to a solution of methyl 6-chloro-5-isobutoxynicotinate (1.84 g) in toluene (25 mL) were added 2-fluoro-5-methoxyphenylboronic acid (2.21 g), tris(dibenzylideneacetone)dipalladium(0) (318 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (570 mg) and 2.0 M aqueous sodium carbonate solution (13.0 mL), and the mixture was stirred at 100° C. for 1 hr. The reaction mixture was filtered through celite, and water was added at room temperature. The reaction mixture was extracted with ethyl acetate, and the extract was washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.82 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-ac99610d5b6540c79654d0e51536658f
Source noteuspto-grants-2015_11