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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1111657생성일: 2026년 10월 24일

Imidazole → Bifonazole

https://huagongshe.com/ko/reaction/1111657

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물Thionyl ChlorideHCID 24386—
반응물alpha-Phenyl[1,1'-biphenyl]-4-methanolHCID 95512—
반응물ThionyldiimidazoleHCID 21946057—
용매AcetonitrileHCID 6342—
생성물BifonazoleHCID 2378—

반응 단계

13.6 g (0.2 mol) of imidazole are dissolved in 150 ml of acetonitrile and 3.5 ml of thionyl chloride are added at 10° C. 13 g (0.05 mol) of (biphenyl-4-yl)-phenyl-carbinol are added to the solution of thionyl-bis-imidazole thus obtained. After standing for 15 hours at room temperature, the solvent is removed by distillation in vacuo. The residue is taken up in chloroform and the solution is washed with water. The organic phase is collected, dried over sodium sulfate and filtered and the solvent is distiller off in vacuo. The oily residue is dissolved in ethyl acetate and freed from insoluble, resinous constituents by filtration. The solvent is again distilled off in vacuo and the residue is purified by recrystallization from acetonitrile. 8.7 g (56% of theory) of (biphenyl-4-yl)-imidazol-1-yl-phenylmethane [alternatively named as diphenyl-imidazolyl-(1)-phenyl-methane or as 1-(α-biphenyl-4-ylbenzyl)imidazole] of melting point 142° C. are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04118487
출처 데이터셋uspto-grants-1978_10
ORD IDord-9b15d528063b40abb29e802c515022ea
출처 메모uspto-grants-1978_10