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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2098185Erstellt: 26. Oktober 2026

1-Naphthaleneacetamide → 2-(naphthalen-1-yl)-N-(thiophen-3-yl)acetamide

https://huagongshe.com/reaction/2098185

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-NaphthaleneacetamideHCID 6861—
EduktPotassium CarbonateHCID 11430—
Edukt1,2-Diaminocyclohexane, trans-HCID 43806—
Edukt3-IodothiopheneHCID 66332—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-(naphthalen-1-yl)-N-(thiophen-3-yl)acetamideHCID 6875551595%

Reaktionsschritte

2-(naphthalen-1-yl)acetamide (14.00 g, 75.6 mmol), 3-iodothiophene (10.15 g, 48.3 mmol), trans-1,2diaminocyclohexane (3.0 ml, 25.0 mmol), cuprous iodide (1.97 g, 10.3 mmol), and potassium carbonate (13.66 g, 98.8 mmol) in dioxane (50 ml) was placed into a preheated oil bath at 95° C. After stirring for 18 h, the heterogenous mixture was diluted with water and extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was flash chromatographed with 19:1, 9:1, 17:3, and 4:1 methylene chloride:ethyl acetate as the eluant to yield 12.26 g (95% yield) of 2-(naphthalen-1-yl)-N-(thiophen-3-yl)acetamide as a brown solid. Method [7] Retention time 2.07 min by HPLC (MH+ 268).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08450363B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-dcf2d6c5651f4a6ba49b55b23785ae7d
Quellennotizuspto-grants-2013_05