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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261967생성일: 2026년 10월 27일

Sodium Chloride → 1-Benzyl-alpha,alpha-bis(p-chlorophenyl)imidazole-2-methanol

https://huagongshe.com/reaction/261967

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물4,4'-DichlorobenzophenoneHCID 7034—
반응물BromobenzeneHCID 7961—
반응물1-BenzylimidazoleHCID 77918—
반응물LithiumHCID 3028194—
반응물HCID 178506676HCID 178506676—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-alpha,alpha-bis(p-chlorophenyl)imidazole-2-methanolHCID 12433938—

반응 단계

A solution of 17.4 g (0.11 mol) of N-benzylimidazole in 40 ml. of anhydrous tetrahydrofuran was added dropwise in the course of one hour, at -20° to -30° C. and under a nitrogen atmosphere, to a phenyl lithium solution, prepared from 1.67 g (0.24 gr. at.) of lithium and 18.8 g (0.12 mol) of bromobenzene in 80 ml. of anhydrous diethyl ether. The mixture was heated for about one hour until a brightly red, homogenous solution was obtained. Subsequently a solution of 25.1 g (0.1 mol) of 4,4'-dichlorobenzophenone in 60 ml. of anhydrous tetrahydrofuran was added in the course of one hour at a temperature between -25° and -15° C. The reaction mixture was stirred for 15 hours at room temperature, under the nitrogen atmosphere and it was then poured on 200 g of ice. The aqueous phase was saturated with sodium chloride and the organic phase was separated off and concentrated. The residue was dissolved in a small amount of acetone and the solution was acidified with 2 N hydrochloric acid. Then some toluene was added and the precipitate formed was filtered off. The product was thrice crystallised from a mixture of isopropyl alcohol and petroleum ether (boiling range 28°-40° C.). 1-Benzyl-α,α-bis(p-chlorophenyl)imidazole-2-methanol was obtained. Melting point 167°-168° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152441
출처 데이터셋uspto-grants-1979_05
ORD IDord-b80c368add57420dbc5a6e50cd05ee63
출처 메모uspto-grants-1979_05