HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949732Generated: October 26, 2026
2-Iodophenol → 3-(2-(2-Iodophenoxy)ethyl)thiophene
https://huagongshe.com/reaction/1949732
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Iodophenol | HCID 10784 | — |
| Reactant | Thiophene-3-ethanol | HCID 83731 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2-(2-Iodophenoxy)ethyl)thiophene | HCID 64084785 | — |
Reaction Steps
To a stirred solution of 2-iodophenol (6.7 g, 30.6 mmol), 2-(3-thienyl)ethanol (3.57 g, 27.8 mol) and triphenylphosphene (8.00 g, 30.6 mmol) in THF, was slowly added a solution of DEAD (4.8 ml, 30.6 mmol). Reaction mixture was stirred at room temperature for 3 hours. Purification on silica gave 3-[2-(2-iodo-phenoxy)-ethyl]-thiophene. A mixture of 3-[2-(2-iodo-phenoxy)-ethyl]-thiophene (1.55 g, 4.69 mmol), palladium(II) acetate (105 mg, 0.47 mmol), potassium carbonate (3.2 g, 23.45 mmol), triphenylphosphene (246 mg, 0.94 mmol) and tetraethylammonium chloride (1.3 g, 4.69 mmol) in DMF was microwaved at 100° C. for 1 hour. The reaction was diluted with dichloromethane and filtered through celite. The filtrate was washed with water, dried (MgSO4), and concentrated in-vacuo. Purification on silica gave 4,5-dihydrobenzo[b]thieno[2,3-d]oxepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399690B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-cbd2413b712a44f9971cb621ba41ba13 |
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| Source note | uspto-grants-2013_03 |
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