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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(2-Ethoxyphenyl)ethanol | HCID 251271 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethoxy-2-(2-iodoethyl)benzene | HCID 89557598 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969557B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-195563b2318b40aeb23418b499615596 |
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| Source note | uspto-grants-2015_03 |
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