Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782313Generated: October 27, 2026

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

https://huagongshe.com/reaction/1782313

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 numberUS07498337B2
Source datasetuspto-grants-2009_03
ORD IDord-207b1b52ece24842853daa73c4e5df6d
Source noteuspto-grants-2009_03