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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1351671Erstellt: 25. Oktober 2026

1-(2-Bromophenyl)ethan-1-ol → (1S)-1-(2-iodophenyl)ethanol

https://huagongshe.com/reaction/1351671

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(2-Bromophenyl)ethan-1-olHCID 6950331—
EduktSodium iodide dihydrateHCID 23685997—
KatalysatorN,N'-DimethylethylenediamineHCID 8070—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt(1S)-1-(2-iodophenyl)ethanolHCID 10514669240,4%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

To each of three identical Emrys microwave reaction vessels was added (S)-1-(2-bromophenyl)ethanol (1.67 g, 8.3 mmol), CuI (189 mg, 1.0 mmol), 1,4-dioxane (12.4 ml), N,N′-dimethylethylenediamine (0.18 ml, 1.7 mmol) and sodium iodide dihydrate (3.1 g, 16.6 mmol). Each vessel was sealed and heated in an Emrys microwave reactor to 150° C. for 2 h. On cooling, the mixtures were combined and partitioned between water (20 ml) and EtOAc (20 ml). The organic phase was washed with brine (20 ml), dried (MgSO4), filtered, and concentrated in vacuo. The crude product was taken up in isohexane (50 ml) and the solution held at −15° C. for 16 h to afford (S)-1-(2-iodophenyl)ethanol as a white crystalline solid (4.95 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07217740B2
Quelldatensatzuspto-grants-2007_05
ORD IDord-753537b8cefe465291c457c56dfc875d
Quellennotizuspto-grants-2007_05