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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646253Generated: October 30, 2026

Iodoethane → 1-Ethyl-4-iodo-2-methanesulfonyl-1H-pyrrole

https://huagongshe.com/reaction/646253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantCesium carbonateHCID 10796—
Reactant4-iodo-2-methanesulfonyl-1H-pyrroleHCID 59772695—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-Ethyl-4-iodo-2-methanesulfonyl-1H-pyrroleHCID 5977271210%

Reaction Steps

A solution of 4-iodo-2-methanesulfonyl-1H-pyrrole (0.14 g, 0.52 mmol) in DMF was treated with Cs2CO3 (0.84 g, 2.58 mmol) and ethyl iodide (0.161 g, 1.03 mmol). The reaction mixture was diluted with EtOAc and washed sequentially with water and brine. The organic phase was separated, dried (Na2SO4) and concentrated in vacuo. Chromatography of the resultant residue (silica gel, 10%-30% EtOAc-hexanes as eluent) yielded an oil; 1H NMR (400 MHz, CDCl3) δ: 1.47 (t, 3H, J=7.3 Hz), 3.09 (s, 3H), 4.26 (q, 2H, J=7.3 Hz), 6.90 (m, 1H), 6.95 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705030B2
Source datasetuspto-grants-2010_04
ORD IDord-e5ac1c5f2e3045679f5546edb5dc95d7
Source noteuspto-grants-2010_04