HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263407Generated: October 31, 2026
Imidazole → 1-(4-Iodobutyl)-4-methoxybenzene
https://huagongshe.com/reaction/263407
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-(4-Methoxyphenyl)butan-1-ol | HCID 97660 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-Iodobutyl)-4-methoxybenzene | HCID 284884 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05643914 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-d9c28a2e46f74787a3d615590b3bb843 |
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| Source note | uspto-grants-1997_07 |
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