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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261937생성일: 2026년 10월 26일

4,4'-Dichlorobenzophenone → alpha,alpha-Bis(p-chlorophenyl)-1-(methoxymethyl)imidazole-2-methanol

https://huagongshe.com/reaction/261937

반응식

참여 물질

역할이름HCID투입량
반응물4,4'-DichlorobenzophenoneHCID 7034—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물1-(methoxymethyl)-1H-imidazoleHCID 88359—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물alpha,alpha-Bis(p-chlorophenyl)-1-(methoxymethyl)imidazole-2-methanolHCID 12433908—

반응 조건

온도-60 °C

반응 단계

To a solution of 11.2 g. (0.1 mol) of 1-(methoxymethyl)-imidazole and 13.9 g. (0.12 mol) of N,N,N',N'-tetramethylethylenediamine in 150 ml. of anhydrous tetrahydrofuran 51 ml. (0.12 mol) of n-butyllithium solution in hexane was added with stirring over a period of about one hour and at a temperature of -60° C. Stirring was continued for another 2 hours at -60° C. Cooling was discontinued and 25.1 g. (0.1 mol) of 4,4'-dichlorobenzophenone in 150 ml. of anhydrous tetrahydrofuran was added drop-wise. The mixture was stirred for 6 hours at room temperature and decomposed by addition of 15 ml. of water. Lithium hydroxide was removed by filtration and the filtrate was concentrated. A 2 N hydrochloric acid solution was added and the mixture was extracted with liberal amounts of diethyl ether. The acidic aqueous solution was made alkaline by addition of potassium carbonate and extracted with diethyl ether, toluene and ethyl acetate. The organic solvent solutions were combined, dried and concentrated. The solid was purified by crystallisation from toluene; its melting point was 145°-146° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152441
출처 데이터셋uspto-grants-1979_05
ORD IDord-65e270d83da04276b7f3ff3d1c3ca2db
출처 메모uspto-grants-1979_05