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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531071Generated: October 30, 2026

Sodium Carbonate → 6-Cyclopropyl-2,2',4'-trifluoro-3-methoxybiphenyl-4-carbaldehyde

https://huagongshe.com/reaction/531071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant6-Bromo-2,2',4'-trifluoro-3-methoxybiphenyl-4-carbaldehydeHCID 117992108—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product6-Cyclopropyl-2,2',4'-trifluoro-3-methoxybiphenyl-4-carbaldehydeHCID 11799223792%

Reaction Conditions

Temperature100 °C

Reaction Steps

Cyclopropylboronic acid (1.01 g), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (0.323 g), a 2 M aqueous sodium carbonate solution (7.87 mL), and tris(dibenzylideneacetone)dipalladium(0) (0.360 g) were added at room temperature to a toluene (30 mL) solution of 6-bromo-2,2′,4′-trifluoro-3-methoxybiphenyl-4-carbaldehyde (1.36 g), and the mixture was stirred at 100° C. for 16 hours in an argon atmosphere. Water was added to the reaction mixture at room temperature, and the mixture was filtered through celite. Then, the filtrate was subjected to extraction with ethyl acetate. The obtained organic layer was washed with water and saturated saline in this order 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 (1.11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353108B2
Source datasetuspto-grants-2016_05
ORD IDord-ea45e0aabcfc43539f69714332526f1f
Source noteuspto-grants-2016_05