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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090714Generated: November 1, 2026

Mesitylene → 5-mesityl-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/2090714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMesityleneHCID 7947—
ReactantCesium carbonateHCID 10796—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant2,4,6-Trimethylbenzeneboronic acidHCID 292184—
Reactant5-bromo-1H-pyrrole-3-carbaldehydeHCID 57831983—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Product5-mesityl-1H-pyrrole-3-carbaldehydeHCID 86630987—

Reaction Steps

A mixture of 5-bromo-1H-pyrrole-3-carbaldehyde (0.87 g), 2,4,6-trimethylphenylboronic acid (3.28 g), cesium carbonate (13.0 g), tri-tert-butylphosphine (0.10 g), tris(dibenzylideneacetone)dipalladium (0) (0.23 g) and mesitylene (200 mL) was stirred with heating under reflux for 5 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=3:1) to give the title compound as a brown amorphous form (yield 0.30 g, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436187B2
Source datasetuspto-grants-2013_05
ORD IDord-87915029b554476b8d80cc469fd68f5c
Source noteuspto-grants-2013_05