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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633719Generated: October 26, 2026

Ammonium Chloride → HCID 178526507, compound

https://huagongshe.com/reaction/1633719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Iodo-1-tritylimidazoleHCID 618252—
Reactant5-Nitro-3,4-dihydronaphthalen-1(2H)-oneHCID 10261946—
ReactantHCID 178418443HCID 178418443—
SolventDichloromethaneHCID 6344—
ProductHCID 178526507HCID 178526507—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503935B1
Source datasetuspto-grants-2003_01
ORD IDord-45768ce4f2fd4507887223018fed9d04
Source noteuspto-grants-2003_01