2-[7-chloro-4-(3-formylphenyl)-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide

Base Information

Chemical Name:2-[7-chloro-4-(3-formylphenyl)-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide
CAS No.:566945-78-6
Molecular Formula:C₂₆H₁₆Cl₂F₃NO₄
Molecular Weight:534.319
Hs Code.:

Synonyms:2-[7-chloro-4-(3-formylphenyl)-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide

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Chemical Property of 2-[7-chloro-4-(3-formylphenyl)-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide

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Technology Process of 2-[7-chloro-4-(3-formylphenyl)-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide

There total 9 articles about 2-[7-chloro-4-(3-formylphenyl)-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide 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:

: 1175754-49-0
2-bromo-5-chloro-4-methylphenol

: 566945-78-6
2-[7-chloro-4-(3-formylphenyl)-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C

1.2: 1 h / -78 °C

1.3: 4 h / Reflux

2.1: triethylamine / tetrahydrofuran / 0.5 h / 0 °C

3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / toluene / 2 h / Reflux

4.1: hydrogenchloride; water; acetic acid / 1 h / Reflux

5.1: oxalyl dichloride; N,N-dimethyl-formamide / tetrahydrofuran / 0.5 h / 20 °C

6.1: tetrahydrofuran / 20 °C

With hydrogenchloride; n-butyllithium; oxalyl dichloride; water; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; hexane; toluene;
DOI:10.1248/cpb.59.1369

Reference yield:

: 1360540-41-5
(4-chloro-2-hydroxy-5-methylphenyl)[3-(1,3-dioxolan-2-yl)phenyl]methanone

: 566945-78-6
2-[7-chloro-4-(3-formylphenyl)-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / tetrahydrofuran / 0.5 h / 0 °C

2: 1,8-diazabicyclo[5.4.0]undec-7-ene / toluene / 2 h / Reflux

3: hydrogenchloride; water; acetic acid / 1 h / Reflux

4: oxalyl dichloride; N,N-dimethyl-formamide / tetrahydrofuran / 0.5 h / 20 °C

5: tetrahydrofuran / 20 °C

With hydrogenchloride; oxalyl dichloride; water; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; toluene;
DOI:10.1248/cpb.59.1369

Reference yield:

: 83803-57-0
1-bromo-4-chloro-2-methoxy-5-methylbenzene

: 566945-78-6
2-[7-chloro-4-(3-formylphenyl)-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: boron tribromide / dichloromethane / -78 - 20 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C

2.2: 1 h / -78 °C

2.3: 4 h / Reflux

3.1: triethylamine / tetrahydrofuran / 0.5 h / 0 °C

4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / toluene / 2 h / Reflux

5.1: hydrogenchloride; water; acetic acid / 1 h / Reflux

6.1: oxalyl dichloride; N,N-dimethyl-formamide / tetrahydrofuran / 0.5 h / 20 °C

7.1: tetrahydrofuran / 20 °C

With hydrogenchloride; n-butyllithium; oxalyl dichloride; water; boron tribromide; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; hexane; dichloromethane; toluene;
DOI:10.1248/cpb.59.1369