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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095304Generated: November 1, 2026

Potassium Iodide → ethyl (1-trityl-1H-imidazol-4-ylmethoxy)acetate

https://huagongshe.com/reaction/1095304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant[1-(triphenylmethyl)-1H-imidazol-4-yl]methanolHCID 382182—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productethyl (1-trityl-1H-imidazol-4-ylmethoxy)acetateHCID 86632954—

Reaction Conditions

Temperature20 °C

Reaction Steps

58.0 mmol of sodium hydride (60% dispersion in paraffin) are added in portions to a solution of 30.0 mmol of (1-trityl-1H-imidazol-4-yl)methanol [33769-07-2] in 300 ml of N,N-dimethylformamide at 20° C. The mixture is stirred at 20° C. for 1.5 hours. 50.0 mmol of ethyl bromoacetate [105-36-2] and 6.00 mmol of potassium iodide are added, and the mixture is stirred at room temperature for 16 hours. A further 58.0 mmol of sodium hydride and 50 mmol of ethyl bromoacetate are added and the mixture is stirred again for 16 hours. The reaction mixture is poured into water and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed with water and brine, dried with magnesium sulphate and evaporated. The title compound is obtained as a brown oil from the residue by flash chromatography (SiO2 60 F). Rf=020 (ethyl acetate-heptane 2:1), Rt=4.32 (gradient I).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138176B2
Source datasetuspto-grants-2012_03
ORD IDord-62186a6ff02f4e0b944be47e4c49ca21
Source noteuspto-grants-2012_03