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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870464Generated: October 25, 2026

Iodine → 2-(2-Ethylphenyl)ethanol

https://huagongshe.com/reaction/870464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantNitrogenHCID 947—
ReactantEthylene OxideHCID 6354—
Reactant1-Bromo-2-ethylbenzeneHCID 16089—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Ethylphenyl)ethanolHCID 1490744763%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 250-mL round-bottom flask protected by N2 was placed tetrahydrofuran (100 mL), Mg (1.0 g, 41.67 mmol, 2.14 equiv) and I2 (0.010 g). Then a solution of 1-bromo-2-ethylbenzene (3.6 g, 19.45 mmol, 1.00 equiv) in THF (15 mL) was added dropwise. The resulting mixture was heated to reflux for 1 h. Then it was cooled to 0° C. and oxirane (50 mL) was added. The resulting solution was stirred at room temperature overnight. The reaction was then quenched by the addition of 20 mL of NH4Cl (aq.). The resulting solution was extracted with 3×50 mL of ethyl acetate and the organic layers combined and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:5). Purification afforded 1.83 g (63%) of 2-(2-ethylphenyl)ethan-1-ol as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969557B2
Source datasetuspto-grants-2015_03
ORD IDord-48ced848e0db4e16a070e5e6ea63278d
Source noteuspto-grants-2015_03