Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642246Generated: November 1, 2026

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

https://huagongshe.com/reaction/642246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-methyl-3-pyrrolecarboxylateHCID 136747—
SolventDimethylformamideHCID 6228—
ProductEthyl 1,2-dimethyl-1H-pyrrole-3-carboxylateHCID 1221151442.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester (7.1 g, 46.05 mmol), iodomethane (5.73 mL, 92.1 mmol) in DMF (50 mL) at 0° C. was added sodium hydride (NaH) (2.39 g, 59.9 mmol, 60% in mineral oil) in one portion, the mixture was stirred at 0° C. for 1 h then the mixture was poured into ice-water (300 mL), extracted with EtOAc, the organic phase was washed with diluted HCl aqueous solution, water and saturated NaCl aqueous solution respectively; the EtOAc layer was then dried over anhydrous sodium sulfate, filtered, concentrated, the residue was purified with column to give a colorless oil, the desired title compound (3.25 g); 1H NMR (200 MHz, CDCl3): δ (ppm)=6.5-6.4 (m, 2H), 4.24 (q, 2H, J=7.1 Hz), 3.52 (s, 3H), 2.49 (s, 3H), 1.33 (t, 3H, J=7.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696223B2
Source datasetuspto-grants-2010_04
ORD IDord-de5fa8f354244e5785950ce525ff8a1e
Source noteuspto-grants-2010_04