(S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propan-1-ol

Base Information

• Chemical Name: (S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propan-1-ol
• CAS No.: 1129692-92-7
• Molecular Formula: C₁₄H₁₃ClF₃N₃O₅
• Molecular Weight: 395.723
• Mol file: 1129692-92-7.mol

Synonyms:(S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propan-1-ol

Chemical Property of (S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propan-1-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propan-1-ol

There total 4 articles about (S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propan-1-ol 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:

Reference yield: 100.0%

1‐[(2S)‐3‐[(tert‐butyldimethylsilyl)oxy]‐2‐{[4‐(trifluoromethoxy)phenyl]methoxy}propyl]‐2‐chloro‐4‐nitro‐1H‐imidazole (1129692-90-5) → (S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propan-1-ol (1129692-92-7)

Guidance literature:

With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 0.5h;

DOI:10.1021/jm801374t

Reference yield:

(S)?1?chloro?3?(2?chloro?4?nitro?1H?imidazol?1?yl)propan?2?ol → (S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propan-1-ol (1129692-92-7)

Guidance literature:

Multi-step reaction with 4 steps

1: sodium hydroxide / 3 h / 90 °C

2: 1H-imidazole / N,N-dimethyl-formamide / 7.67 h / 20 °C

3: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran / 4.5 h / 0 - 20 °C / Inert atmosphere

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 20 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium hydroxide; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

(S)?3?(2?chloro?4?nitro?1H?imidazol?1?yl)propane?1,2?diol → (S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propan-1-ol (1129692-92-7)

Guidance literature:

Multi-step reaction with 3 steps

1: 1H-imidazole / N,N-dimethyl-formamide / 7.67 h / 20 °C

2: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran / 4.5 h / 0 - 20 °C / Inert atmosphere

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 20 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;

upstream raw materials:

1‐[(2S)‐3‐[(tert‐butyldimethylsilyl)oxy]‐2‐{[4‐(trifluoromethoxy)phenyl]methoxy}propyl]‐2‐chloro‐4‐nitro‐1H‐imidazole

(S)?1?(tert?butyldimethylsilyloxy)?3?(2?chloro?4?nitro?1H?imidazol?1?yl) propan?2?ol

Downstream raw materials:

(S)-2-(4-(trifluoromethoxy)benzyloxy)-3-(2-chloro-4-nitro-1H-imidazol-1-yl)propyl methanesulfonate