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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76162Erstellt: 25. Oktober 2026

Sodium Iodide → N-(1-(4-Iodophenyl)propan-2-YL)acetamide

https://huagongshe.com/reaction/76162

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktN,N'-DimethylethylenediamineHCID 8070—
EduktN-(1-(4-bromophenyl)propan-2-yl)acetamideHCID 45824256—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-(1-(4-Iodophenyl)propan-2-YL)acetamideHCID 66611344—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To 6.00 g (23.4 mmol) N-(1-(4-bromophenyl)propan-2-yl)acetamide (I44.1) in 65 mL dioxan are added 0.45 g (2.34 mmol) CuI, 0.50 mL (4.70 mmol) N,N′-dimethylethylendiamine and 7.02 g (46.9 mmol) NaI. The reaction mixture is stirred at 120° C. for 70 h. The mixture is allowed to cool to r.t. and half of the solvent is removed in vacuo. EtOAc and diluted aq. ammonia solution are added and the layers are separated. The aq. layer is once more extracted with EtOAc. The organic layers are combined, dried with Na2SO4 and the solvent is removed in vacuo. The crude product is triturated with diethylether and dried at 50° C. in vacuo.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835472B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-0f307e46944d4233a87b6d58561972ae
Quellennotizuspto-grants-2014_09