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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295744Generated: October 30, 2026

Dimethylformamide → HCID 86602426, compound

https://huagongshe.com/reaction/1295744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1H-Pyrrole, 3-methyl-HCID 12023—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium AcetateHCID 517045—
Reactant3-methyl-1H-pyrrole-2-carbaldehydeHCID 11423566—
Reactant4-Methyl-1H-pyrrole-2-carbaldehydeHCID 14116047—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductHCID 86602426HCID 86602426—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 3.15 ml (41 mmol) of DMF at 0° C. under argon was added dropwise 3.81 ml (41 mmol) of phosphorus oxychloride. The cooling bath was removed and stirring was continued for 15 min. The solution was diluted with 9 ml of 1,2-dichloroethane and again cooled to 0° C. A solution of 3.0 g (37 mmol) of 3-methylpyrrole in 9 ml of 1,2-dichloroethane was added dropwise. The mixture was heated to reflux for 15 min, cooled to 0° C. and a solution of 16.2 g (203 mmol) of sodium acetate in 45 ml of water was added with vigorous stirring. The mixture was heated at reflux for 20 min and allowed to cool to room temperature. The aqueous layer was separated and extracted twice with methylene chloride. The combined organic layers were washed with sat NaHCO3 until pH 7, dried (MgSO4), and the solvent removed to yield a dark oily solid which was purified by flash chromatography (10% EtOAc:hexane) to afford 3.6 g (89%) of a 4:1 mixture of 2-formyl-3-methylpyrrole and 2-formyl-4-methylpyrrole as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244733B2
Source datasetuspto-grants-2007_07
ORD IDord-711e0c3dcac248009339b7325ba9371e
Source noteuspto-grants-2007_07