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4-(tert-butyldimethylsilylperoxy)-4-(4-fluorophenyl)-2-phenyl-5-[4-(trifluoromethyl)phenyl]-4H-isoimidazole

Base Information
  • Chemical Name:4-(tert-butyldimethylsilylperoxy)-4-(4-fluorophenyl)-2-phenyl-5-[4-(trifluoromethyl)phenyl]-4H-isoimidazole
  • CAS No.:1594937-33-3
  • Molecular Formula:C28H28F4N2O2Si
  • Molecular Weight:528.622
  • Hs Code.:
4-(tert-butyldimethylsilylperoxy)-4-(4-fluorophenyl)-2-phenyl-5-[4-(trifluoromethyl)phenyl]-4H-isoimidazole

Synonyms:4-(tert-butyldimethylsilylperoxy)-4-(4-fluorophenyl)-2-phenyl-5-[4-(trifluoromethyl)phenyl]-4H-isoimidazole

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Chemical Property of 4-(tert-butyldimethylsilylperoxy)-4-(4-fluorophenyl)-2-phenyl-5-[4-(trifluoromethyl)phenyl]-4H-isoimidazole
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Technology Process of 4-(tert-butyldimethylsilylperoxy)-4-(4-fluorophenyl)-2-phenyl-5-[4-(trifluoromethyl)phenyl]-4H-isoimidazole

There total 5 articles about 4-(tert-butyldimethylsilylperoxy)-4-(4-fluorophenyl)-2-phenyl-5-[4-(trifluoromethyl)phenyl]-4H-isoimidazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
5-(4-fluorophenyl)-2-phenyl-4-[4-(trifluoromethyl)phenyl]imidazole; With oxygen; methylene blue; In methanol; dichloromethane; at -78 ℃; for 1.5h;
tert-butyldimethylsilyl chloride; With 1H-imidazole; In pyridine; at 0 ℃; for 0.333333h;
In hexane; isopropyl alcohol;
DOI:10.1002/ejoc.201300976
Guidance literature:
Multi-step reaction with 4 steps
1.1: magnesium / diethyl ether / 3 h / Reflux
2.1: selenium(IV) oxide / acetic acid / 3 h / Reflux
3.1: ammonium acetate / acetic acid / Reflux; Inert atmosphere
4.1: methylene blue; oxygen / dichloromethane; methanol / 1.5 h / -78 °C
4.2: 0.33 h / 0 °C
4.3: Daicel Chiralpak AD-H column
With selenium(IV) oxide; ammonium acetate; oxygen; methylene blue; magnesium; In methanol; diethyl ether; dichloromethane; acetic acid;
DOI:10.1002/ejoc.201300976
Guidance literature:
Multi-step reaction with 3 steps
1.1: selenium(IV) oxide / acetic acid / 3 h / Reflux
2.1: ammonium acetate / acetic acid / Reflux; Inert atmosphere
3.1: methylene blue; oxygen / dichloromethane; methanol / 1.5 h / -78 °C
3.2: 0.33 h / 0 °C
3.3: Daicel Chiralpak AD-H column
With selenium(IV) oxide; ammonium acetate; oxygen; methylene blue; In methanol; dichloromethane; acetic acid;
DOI:10.1002/ejoc.201300976
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