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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604020Generated: November 2, 2026

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

https://huagongshe.com/reaction/1604020

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), 1.60 (m, 2H, CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990314
Source datasetuspto-grants-1999_11
ORD IDord-d265d29acfb04d728d809314457b56d2
Source noteuspto-grants-1999_11