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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220470Generated: November 1, 2026

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

https://huagongshe.com/reaction/2220470

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 numberUS07417047B2
Source datasetuspto-grants-2008_08
ORD IDord-ade7447284d349bebb795c3e66dd894d
Source noteuspto-grants-2008_08