Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078837Generated: October 26, 2026

2-Iodophenol → 3-(2-(2-Iodophenoxy)ethyl)thiophene

https://huagongshe.com/reaction/2078837

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 numberUS07928248B2
Source datasetuspto-grants-2011_04
ORD IDord-1cf4794d4287474796075a712f272264
Source noteuspto-grants-2011_04