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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070391Generated: October 26, 2026

Sodium Carbonate → 4-Methyl-5-phenyl-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/2070391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
ReactantPhenylboronic AcidHCID 66827—
Reactant5-bromo-4-methyl-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 86232734—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-Methyl-5-phenyl-1H-pyrrole-3-carbaldehydeHCID 7136281281.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 5-bromo-4-methyl-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde (1.78 g), phenylboronic acid (1.37 g), dichloro[bis(triphenylphosphine)]palladium (0.19 g) and sodium carbonate (1.72 g) in 1,2-dimethoxyethane (30 mL)-water (10 mL) was stirred at 100° C. for 1 hr. 8 mol/L aqueous sodium hydroxide solution (15 mL) was added, and the mixture was stirred at 90° C. for 3 hr. After cooling, 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=9:1→1:1), and the obtained solid was washed with hexane to give the title compound as a pale-yellow solid (yield 815 mg, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299261B2
Source datasetuspto-grants-2012_10
ORD IDord-101debb2c93c41c8a03748baf84dd256
Source noteuspto-grants-2012_10