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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodophenolHCID 10784—
ReactantThiophene-3-ethanolHCID 83731—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTetrahydrofuranHCID 8028—
Product3-(2-(2-Iodophenoxy)ethyl)thiopheneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399690B2
Source datasetuspto-grants-2013_03
ORD IDord-cbd2413b712a44f9971cb621ba41ba13
Source noteuspto-grants-2013_03