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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197213Generated: October 29, 2026

1,2-Dimethoxyethane → 5-(2-fluoropyridin-3-yl)-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/2197213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Fluoropyridine-3-boronic acidHCID 2783270—
Reactant5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 86232805—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product5-(2-fluoropyridin-3-yl)-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 8662397468%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde (3.15 g), (2-fluoropyridin-3-yl)boronic acid (2.83 g), sodium hydrogencarbonate (2.53 g) and tetrakis(triphenylphosphine)palladium (870 mg) were added to a degassed mixture of 1,2-dimethoxyethane (80 mL) and water (20 mL), and the mixture was stirred under a nitrogen atmosphere at 80° C. for 5 hr. The reaction mixture was allowed to cool, a saturated aqueous sodium hydrogencarbonate solution was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→2:3) to give the title compound as a colorless oil (yield 2.25 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338462B2
Source datasetuspto-grants-2012_12
ORD IDord-c11475869c3046bf89f99f5057f1a67d
Source noteuspto-grants-2012_12