ethyl [1-benzhydryl-2-({[tert-butyl(diphenyl)silyl]oxy}ethyl)-5-chloro-1H-indol-3-yl](oxo)acetate

Base Information

Chemical Name:ethyl [1-benzhydryl-2-({[tert-butyl(diphenyl)silyl]oxy}ethyl)-5-chloro-1H-indol-3-yl](oxo)acetate
CAS No.:540524-33-2
Molecular Formula:C₄₃H₄₂ClNO₄Si
Molecular Weight:700.349
Hs Code.:

Synonyms:ethyl [1-benzhydryl-2-({[tert-butyl(diphenyl)silyl]oxy}ethyl)-5-chloro-1H-indol-3-yl](oxo)acetate

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Chemical Property of ethyl [1-benzhydryl-2-({[tert-butyl(diphenyl)silyl]oxy}ethyl)-5-chloro-1H-indol-3-yl](oxo)acetate

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Technology Process of ethyl [1-benzhydryl-2-({[tert-butyl(diphenyl)silyl]oxy}ethyl)-5-chloro-1H-indol-3-yl](oxo)acetate

There total 5 articles about ethyl [1-benzhydryl-2-({[tert-butyl(diphenyl)silyl]oxy}ethyl)-5-chloro-1H-indol-3-yl](oxo)acetate 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:

: 540522-60-9
N-(2-bromo-4-chlorophenyl)-2,2,2-trifluoroacetamide

: 540524-33-2
ethyl [1-benzhydryl-2-({[tert-butyl(diphenyl)silyl]oxy}ethyl)-5-chloro-1H-indol-3-yl](oxo)acetate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / N,N-dimethyl-formamide / 4 h / 120 °C / Sealed tube; Inert atmosphere

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

3: triethylamine / diethyl ether

4: caesium carbonate / acetonitrile / 2 h / Reflux

With 1H-imidazole; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; caesium carbonate; triethylamine; In diethyl ether; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 873-38-1
4-chloro-2-bromoaniline

: 540524-33-2
ethyl [1-benzhydryl-2-({[tert-butyl(diphenyl)silyl]oxy}ethyl)-5-chloro-1H-indol-3-yl](oxo)acetate

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane / 1 h / 20 °C

2: triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / N,N-dimethyl-formamide / 4 h / 120 °C / Sealed tube; Inert atmosphere

3: 1H-imidazole / N,N-dimethyl-formamide / 20 °C

4: triethylamine / diethyl ether

5: caesium carbonate / acetonitrile / 2 h / Reflux

With 1H-imidazole; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; caesium carbonate; triethylamine; In diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 540522-61-0
2-(5-chloro-1H-indol-2-yl)ethanol

: 540524-33-2
ethyl [1-benzhydryl-2-({[tert-butyl(diphenyl)silyl]oxy}ethyl)-5-chloro-1H-indol-3-yl](oxo)acetate

Guidance literature:: Multi-step reaction with 3 steps

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

2: triethylamine / diethyl ether

3: caesium carbonate / acetonitrile / 2 h / Reflux

With 1H-imidazole; caesium carbonate; triethylamine; In diethyl ether; N,N-dimethyl-formamide; acetonitrile;