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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 392582Erstellt: 25. Oktober 2026

Ammonium Chloride → (6-ethoxynaphthalen-2-yl)(1-trityl-1H-imidazol-4-yl)methanol

https://huagongshe.com/reaction/392582

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt2-Bromo-6-ethoxynaphthaleneHCID 236858—
Edukt1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
EduktMagnesiumHCID 5462224—
KatalysatorMethyl iodideHCID 6328—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(6-ethoxynaphthalen-2-yl)(1-trityl-1H-imidazol-4-yl)methanolHCID 2266497559,6%

Reaktionsschritte

2-Bromo-6-ethoxynaphthalene (5.3 g) was dissolved in THF (40 ml) and magnesium (0.515 g) and methyl iodide (one drop) were added and the mixture was vigorously stirred to dissolve magnesium. The reaction mixture was ice-cooled and a solution of 4-formyl-1-tritylimidazole (7 g) in THF (80 ml) was added dropwise over 30 min. The mixture was stirred at room temperature for 1 h. To the reaction mixture were added saturated aqueous solution (40 ml) of ammonium chloride and water (40 ml) and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate and concentrated. The residue was washed with ethyl acetate to give (6-ethoxynaphthalen-2-yl)-(1-trityl-1H-imidazol-4-yl)methanol (6.3 g) as a colorless powder. This product (6.3 g) was dissolved in dichloromethane (120 ml) and manganese dioxide (6 g) was added. The mixture was stirred at room temperature overnight. The reaction mixture was filtered through Celite and the filtrate was concentrated. The residue was crystallized from THF-ethyl acetate to give the title compound (5.5 g) as a colorless powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06800778B1
Quelldatensatzuspto-grants-2004_10
ORD IDord-bbb43dea9230438392dc61435eab668f
Quellennotizuspto-grants-2004_10