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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Edukt | N-(1-(4-bromophenyl)propan-2-yl)acetamide | HCID 45824256 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | N-(1-(4-Iodophenyl)propan-2-YL)acetamide | HCID 66611344 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835472B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-0f307e46944d4233a87b6d58561972ae |
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| Quellennotiz | uspto-grants-2014_09 |
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