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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1633719Erstellt: 25. Oktober 2026

Ammonium Chloride → HCID 178526507, Verbindung

https://huagongshe.com/reaction/1633719

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt4-Iodo-1-tritylimidazoleHCID 618252—
Edukt5-Nitro-3,4-dihydronaphthalen-1(2H)-oneHCID 10261946—
EduktHCID 178418443HCID 178418443—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178526507HCID 178526507—

Reaktionsschritte

A solution of 4-iodo-1-trityl-1H-imidazole (5.5 g, 13 mmol) (prepared as described by Kirk, K. J. Heterocyclic Chem. (1985), 22, 57-59) in dichloromethane (50 mL) was treated with ethylmagnesium bromide (3.0 M in diethyl ether, 4.2 mL) over 4 minutes, stirred for 30 minutes, treated with 5-nitrotetralone (prepared as described by Zhang, M J. Amer. Chem. SoC, (1994), 116, 4852-4857), stirred for 6 hours, treated with ammonium chloride solution (50 mL) and extracted with a mixture of diethyl ether (300 mL) and ethyl acetate (50 mL). The organic layer was isolated, treated with dichloromethane (500 mL) to dissolve the product which started to crystallize, dried (MgSO4), filtered, concentrated, treated with trifluoroacetic acid (80 mL), stirred for 48 hours, concentrated to an oil, neutralized with sodium bicarbonate solution and extracted twice with dichloromethane. The combined dichloromethane layers were dried (MgSO4), filtered and concentrated. The residue was purified on silica gel with a gradient of 5%-10% methanol/dichloromethane to provide the desired compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06503935B1
Quelldatensatzuspto-grants-2003_01
ORD IDord-45768ce4f2fd4507887223018fed9d04
Quellennotizuspto-grants-2003_01