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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261951Generated: November 3, 2026

Ammonia → alpha,alpha-Bis(p-chlorophenyl)-1-(methoxymethyl)-4,5-dimethylimidazole-2-methanol

https://huagongshe.com/reaction/261951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4,4'-DichlorobenzophenoneHCID 7034—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1-(Methoxymethyl)-4,5-dimethylimidazoleHCID 21321308—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Productalpha,alpha-Bis(p-chlorophenyl)-1-(methoxymethyl)-4,5-dimethylimidazole-2-methanolHCID 12433910—

Reaction Steps

At a temperature of -60° C. and under a nitrogen atmosphere, 114 ml. (0.24 mol) of butyllithium solution (20% in hexane) were added drop-wise with stirring to a solution of 28 g. (0.20 mol) of 1-(methoxymethyl)-4,5-dimethylimidazole and 28 g. (0.24 mol) of N,N,N',N'-tetramethylethylenediamine in 200 ml. of anhydrous tetrahydrofuran. After 2 hours stirring, 50 g. (0.20 mol) of 4,4'-dichlorobenzophenone in 250 ml of anhydrous tetrahydrofuran were added drop-wise at -60° C. After being kept standing overnight, the reaction mixture was extracted with water and the organic phase was concentrated by distilling off the solvents. The residue was treated with 2 N hydrochloric acid and diethyl ether, which resulted in the formation of an organic and aqueous layer with an oily intermediate layer. The aqueous and oily layers were made alkaline with ammonia and extracted with diethyl ether. The extract was dried over sodium sulphate and the solvent was distilled off. The oily residue was thrice recrystallised from isopropyl alcohol. α,α-Bis(p-chlorophenyl)-1-(methoxymethyl)-4,5-dimethylimidazole-2-methanol was obtained. Melting point 151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152441
Source datasetuspto-grants-1979_05
ORD IDord-547f966556234a8d96bd5da76264c1fe
Source noteuspto-grants-1979_05