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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723235Generated: October 31, 2026

Ethyl Acetate → 4-Iodo-5-methyl-1H-benzoimidazole

https://huagongshe.com/reaction/723235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant5-MethylbenzimidazoleHCID 11979—
ReactantN-IodosuccinimideHCID 120273—
ReactantSodium BicarbonateHCID 516892—
SolventTrifluoroacetic acidHCID 6422—
Product4-Iodo-5-methyl-1H-benzoimidazoleHCID 2188639430.2%

Reaction Steps

A solution of 5-methyl-1H-benzoimidazole (132 mg, 1.0 mmol) and NIS (248 mg, 1.10 mmol) in 1 mL of TFA was reflux for 1 hr and then cooled to RT. Treated with 30 mL of EtOAc, the mixture was neutralized with sat. NaHCO3 solution. The organic layer was washed with H2O (10 mL), brine (10 mL) and dried (Na2SO4). Removal of the solvent under reduced pressure followed by flash chromatography of the residue on silica gel (5% MeOH/CH2Cl2) gave 78 mg (30%) of product as a white solid: 1H-NMR (CDCl3; 400 MHz) δ 8.07 (d, 1H), 7.57 (br s, 1H), 7.22 (d, 1H, J. 8.4 Hz), 2.59 (s, 3H). Mass spectrum (ESI, m/z): Calcd. for C8H7IN2, 259.0 (M+H), found 259.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138530B2
Source datasetuspto-grants-2006_11
ORD IDord-ac87af7ff7c34219a70567ee909e8579
Source noteuspto-grants-2006_11