Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518915Generated: October 31, 2026

Methyl iodide → Ethyl 1,2-dimethyl-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/518915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-methyl-3-pyrrolecarboxylateHCID 136747—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 1,2-dimethyl-1H-pyrrole-3-carboxylateHCID 12211514—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 10 g of ethyl 2-methyl-1H-pyrrole-3-carboxylate (65.3 mmol) and 8.95 mL (130.6 mmol) of methyl iodide in 70 mL of dimethylformamide placed at 0° C. there are added, in three portions, 2.61 g (65.3 mmol) of sodium hydride 60%. The batch is then stirred at 0° C. for 1 hour. Then, the reaction mixture is hydrolysed by the addition of 420 mL of ice-cold water. The reaction mixture is then diluted with ethyl acetate, successively washed with 0.1M HCl solution, saturated aqueous LiCl solution and then brine. The organic phase is then dried over MgSO4, filtered, concentrated to dryness and purified by chromatography over silica gel (petroleum ether/AcOEt gradient).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115159B2
Source datasetuspto-grants-2015_08
ORD IDord-2b85008782ed40f69d0258f7944edc6f
Source noteuspto-grants-2015_08