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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4,4'-Dichlorobenzophenone | HCID 7034 | — |
| 반응물 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 반응물 | 1-(methoxymethyl)-1H-imidazole | HCID 88359 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | alpha,alpha-Bis(p-chlorophenyl)-1-(methoxymethyl)imidazole-2-methanol | HCID 12433908 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04152441 |
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| 출처 데이터셋 | uspto-grants-1979_05 |
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| ORD ID | ord-65e270d83da04276b7f3ff3d1c3ca2db |
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| 출처 메모 | uspto-grants-1979_05 |
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