Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 84469Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/84469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-IodophenolHCID 10784—
EduktThiophene-3-ethanolHCID 83731—
EduktDiethyl azodicarboxylateHCID 5462977—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(2-(2-Iodophenoxy)ethyl)thiopheneHCID 64084785—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846762B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-558fc451011e4d648d8c02d6fa52669b
Quellennotizuspto-grants-2014_09