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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261935생성일: 2026년 10월 27일

4-Chlorobenzophenone → 1-[(Benzyloxy)methyl]-alpha-(p-chlorophenyl)-alpha-phenylimidazole-2-methanol

https://huagongshe.com/reaction/261935

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorobenzophenoneHCID 8653—
반응물1-BenzyloxymethylimidazoleHCID 14795908—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물1-[(Benzyloxy)methyl]-alpha-(p-chlorophenyl)-alpha-phenylimidazole-2-methanolHCID 12433915—

반응 단계

To a solution of 11.8 g. of 1-[(benzyloxy)methyl]imidazole in 100 ml. of anhydrous tetrahydrofuran and 50 ml. of anhydrous diethyl ether a solution of 38 ml. of a 20% butyllithium suspension in hexane dissolved in 75 ml. of anhydrous diethyl ether was added drop-wise with stirring at room temperature. Thereafter a solution of 14.6 g. of 4-chlorobenzophenone in 100 ml. of anhydrous tetrahydrofuran and 50 ml. of anhydrous diethyl ether was added drop-wise at room temperature. The mixture was kept for three hours and then extracted with a dilute acid solution. The acidic aqueous layer was made alkaline with 2 N sodium hydroxide solution and extracted with diethyl ether. Part of the ether was removed by evaporation and the residue washed with water. The ether solution was again concentrated and the desired compound crystallised from a mixture of toluene and petroleum ether (boiling range 28°-40° C.). Melting point of the product was 114.5°-117° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152441
출처 데이터셋uspto-grants-1979_05
ORD IDord-39d68689ec82426b914e67b3c5e74115
출처 메모uspto-grants-1979_05