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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351667Erstellt: 24. Oktober 2026

1,4-Dioxane → 1-Amino-4-[3-(morpholin-4-yl)phenyl]naphthalene

https://huagongshe.com/de/reaction/351667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DioxaneHCID 31275—
Edukt4-Bromo-1-naphthylamineHCID 75303—
KatalysatorHCID 178418397HCID 178418397—
Produkt1-Amino-4-[3-(morpholin-4-yl)phenyl]naphthaleneHCID 1208527538%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

The above intermediate (1.49 g, 3.51 mmol) and 1-amino-4-bromonaphthalene (0.69 g, 3.11 mmol) were dissolved in 20 mL anhydrous 1,4-dioxane in a sealable tube under inert gas atmosphere. The solution was degased and purged with nitrogen (2×). Tetrakis(triphenylphosphine)palladium(0) (0.21 g, 0.18 mmol) was added and the solution was degassed and purged with nitrogen again (2×). The tube was sealed and heated to 100° C. for 17 h. After cooling to room temperature the mixture was diluted with EtOAc, saturated aqueous potassium carbonate solution (10 mL) was added and the mixture was stirred for 1 h at room temperature. The mixture was filtered over diatomaceous earth and the layers were separated. The aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4), filtered and evaporated to dryness. Purification of the residue by flash chromatography afforded 0.363 g (1.19 mmol, 38%) of title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743788B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-f8a3525846e6472391e56daff4f1a631
Quellennotizuspto-grants-2004_06