돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1111658생성일: 2026년 10월 24일

Trityl chloride → Bifonazole

https://huagongshe.com/ko/reaction/1111658

반응식

참여 물질

역할이름HCID투입량
반응물Trityl chlorideHCID 6456—
반응물4-(Chlorophenylmethyl)-1,1'-biphenylHCID 111006—
반응물TMS-ImidazoleHCID 14420972—
용매AcetonitrileHCID 6342—
생성물BifonazoleHCID 237852.1%

반응 단계

167 g (0.6 mol) of biphenyl-4-yl-phenyl-chloromethane [alternatively named as diphenyl-phenyl-chloromethane or as α-(biphenyl-4-yl)benzyl chloride] and 92 g (0.66 mol) of trimethylsilylimidazole, dissolved in 500 ml of acetonitrile, are heated under reflux for 15 hours. After distilling off the solvent, the crystalline residue is purified by recrystallization from ethyl acetate. 97 g (52% of theory) of (biphenyl-4-yl)-imidazol-1-yl-phenylmethane 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-5bffc8abda5f4c0ba78b60f58d66befa
출처 메모uspto-grants-1978_10