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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870468Generated: October 25, 2026

Imidazole → 1-Ethoxy-2-(2-iodoethyl)benzene

https://huagongshe.com/reaction/870468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(2-Ethoxyphenyl)ethanolHCID 251271—
SolventDichloromethaneHCID 6344—
Product1-Ethoxy-2-(2-iodoethyl)benzeneHCID 8955759861%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 50-mL round-bottom flask was placed dichloromethane (20 mL) and 2-(2-ethoxyphenyl)ethan-1-ol (1.33 g, 8.00 mmol, 1.00 equiv). The solution was cooled to 0° C. in a water/ice bath. Then PPh3 (2.72 g, 10.37 mmol, 1.30 equiv), imidazole (707 mg, 10.40 mmol, 1.30 equiv) and I2 (2.44 g, 9.61 mmol, 1.20 equiv) were added. The resulting solution was stirred at room temperature overnight. The reaction was then quenched by the addition of 50 mL of NaHSO3 (aq.). The organic layer was separated and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (0:100). Purification afforded 1.34 g (61%) of 1-ethoxy-2-(2-iodoethyl)benzene as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969557B2
Source datasetuspto-grants-2015_03
ORD IDord-195563b2318b40aeb23418b499615596
Source noteuspto-grants-2015_03