sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate

Base Information

Chemical Name:sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate
CAS No.:1428127-90-5
Molecular Formula:C₂₅H₁₉Cl₂FNO₄*Na
Molecular Weight:510.324
Hs Code.:

Synonyms:sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate

Suppliers and Price of sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate

There total 6 articles about sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate 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: 83.0%

: 1428129-94-5
1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3,4-dihydrooxepino[5,4,3-cd]indol-6(1H)-one

: 1428127-90-5
sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate

Guidance literature:: With sodium hydroxide; In ethanol; water; at 80 ℃; for 1h;

Reference yield:

: 1427422-74-9
2-(bromomethyl)-4-chloro-1-((4-chloro-2-fluorobenzyl)oxy)benzene

: 1428127-90-5
sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.25 h / 0 °C / Inert atmosphere

1.2: 1.5 h / 0 °C

2.1: sodium hexamethyldisilazane / toluene / 0.33 h / 0 °C / Inert atmosphere

2.2: 2 h / 20 °C

3.1: hydrogenchloride / acetone / 1 h / 50 °C

4.1: sodium tetrahydroborate / tetrahydrofuran / 1 h / 20 °C

5.1: sodium hydroxide / ethanol; water / 1 h / 80 °C

With hydrogenchloride; sodium tetrahydroborate; sodium hexamethyldisilazane; sodium hydride; sodium hydroxide; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetone; toluene; mineral oil;

Reference yield:

: 53462-88-7
3-Formylindole-4-carboxylic acid methyl ester

: 1428127-90-5
sodium 1-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)-3-(2-hydroxyethyl)-1H-indole-4-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.25 h / 0 °C / Inert atmosphere

1.2: 1.5 h / 0 °C

2.1: sodium hexamethyldisilazane / toluene / 0.33 h / 0 °C / Inert atmosphere

2.2: 2 h / 20 °C

3.1: hydrogenchloride / acetone / 1 h / 50 °C

4.1: sodium tetrahydroborate / tetrahydrofuran / 1 h / 20 °C

5.1: sodium hydroxide / ethanol; water / 1 h / 80 °C

With hydrogenchloride; sodium tetrahydroborate; sodium hexamethyldisilazane; sodium hydride; sodium hydroxide; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetone; toluene; mineral oil;