5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione

Base Information

• Chemical Name: 5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione
• CAS No.: 1186116-08-4
• Molecular Formula: C₂₇H₂₇F₃N₂O₅
• Molecular Weight: 516.517

Synonyms:5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione

Chemical Property of 5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione

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Technology Process of 5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione

There total 5 articles about 5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione 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:

7-(4-bromobutoxy)-8-n-propyl-4-(trifluoromethyl)-2H-chromen-2-one (1186116-44-8) + 5-methyl-5-phenylimidazolidin-2,4-dione (6843-49-8,27539-12-4,99571-24-1,101693-73-6) → 5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione (1186116-08-4)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 16h;

DOI:10.1016/j.bmcl.2015.01.047

Reference yield:

1,3-Dimethoxy-2-(prop-1'-yl)benzene (16929-64-9) → 5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione (1186116-08-4)

Guidance literature:

Multi-step reaction with 4 steps

1: boron tribromide / dichloromethane / 3.75 h / -70 - 20 °C

2: zinc(II) chloride / 18 h / 110 °C

3: potassium carbonate / N,N-dimethyl-formamide / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

With boron tribromide; potassium carbonate; zinc(II) chloride; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2015.01.047

Reference yield:

7-hydroxy-8-n-propyl-4-(trifluoromethyl)-2H-chromen-2-one (194855-25-9) → 5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione (1186116-08-4)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

With potassium carbonate; In N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2015.01.047

upstream raw materials:

7-hydroxy-8-n-propyl-4-(trifluoromethyl)-2H-chromen-2-one

1,3-Dimethoxybenzene

1,3-Dimethoxy-2-(prop-1'-yl)benzene

2-propyl-1,3-benzenediol

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