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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088464Generated: November 3, 2026

2,5-Hexanedione → HCID 43806226, compound

https://huagongshe.com/reaction/2088464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-HexanedioneHCID 8035—
Reactant5-Bromo-o-toluidineHCID 2734805—
CatalystHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 43806226HCID 4380622660%

Reaction Steps

To a solution 5-bromo-2-methyl aniline (6.38 g, 36.74 mmol) in EtOH (30 ml) was added acetonyl acetone (5.0 ml, 42.62 mmol) and one drop of conc. aqueous HCl. The mixture was heated at reflux for 18 h and then cooled. Solvent was evaporated to dryness under reduced pressure and the residue was partitioned between water and EtOAc. The organic layer was separated and washed with water and brine dried over MgSO4, filtered and concentrated to dryness under reduced pressure. Purification of the residue by flash chromatography (hex:EtOAc/8:2) gave 5.8 g of 1-(5-bromo-2-methyl-phenyl)-2,5-dimethyl-1H-pyrrole (60%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435990B2
Source datasetuspto-grants-2013_05
ORD IDord-8fa8ea46db214686a96f1d956892eb65
Source noteuspto-grants-2013_05