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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263407Generated: October 31, 2026

Imidazole → 1-(4-Iodobutyl)-4-methoxybenzene

https://huagongshe.com/reaction/263407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant4-(4-Methoxyphenyl)butan-1-olHCID 97660—
SolventTolueneHCID 1140—
Product1-(4-Iodobutyl)-4-methoxybenzeneHCID 284884—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a stirred solution of 4-(4-methoxyphenyl)butan-1-ol (9.37 g, 52 mmol, Aldrich) in dry toluene (185 mL) under an argon atmosphere was added triphenylphosphine (17.8 g, 67.6 mmol) and imidazole (10.6 g, 156 mmol). After ten minutes I2 (17.1 g, 67.6 mmol) was added. The reaction was then heated at 65 ° C. for 30 minutes. Upon cooling to room temperature the reaction was concentrated to 1/4 volume. The remaining solution was diluted with Et2O and washed with H2O and brine and dried (MgSO4). The solvent was removed and the resulting residue was dissolved in CH2Cl2 and applied to a flash chromatography column (silica). Elution with 2% EtOAc in hexane provided a colorless oil: 1H NMR (250 MHz, CDCl3) δ7.08 (d, J=8.7 Hz, 2H, phenyl), 6.82 (d, J=8.7 Hz, 2H, phenyl), 3.78 (s, 3H, OMe), 3.17 (t, J=7.4 Hz, 2H, I-CH2), 2.54 (t, J=7.2 Hz, 2H, benzylic), 1.85 (m, 2H, CH2), 160 (m, 2H, CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05643914
Source datasetuspto-grants-1997_07
ORD IDord-d9c28a2e46f74787a3d615590b3bb843
Source noteuspto-grants-1997_07