ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-carboxylate

Base Information

Chemical Name:ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-carboxylate
CAS No.:1418287-68-9
Molecular Formula:C₂₆H₂₉BF₃NO₆
Molecular Weight:519.326
Hs Code.:

Synonyms:ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-carboxylate

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Chemical Property of ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-carboxylate

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Technology Process of ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-carboxylate

There total 5 articles about ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-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:

: 1418287-67-8
ethyl 5-bromo-1-{2-[4-(trifluoromethoxy)phenoxy]ethyl}-1H-indole-2-carboxylate

: 25015-63-8
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane

: 1418287-68-9
ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-carboxylate

Guidance literature:: With potassium acetate; palladium diacetate; XPhos; In 1,4-dioxane; at 85 ℃; Inert atmosphere;

Reference yield:

: 627902-05-0
2-[4-(trifluoromethoxy)phenoxy]ethanol

: 1418287-68-9
ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / toluene / 0 - 20 °C

2: potassium acetate; palladium diacetate; XPhos / 1,4-dioxane / 85 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; potassium acetate; palladium diacetate; triphenylphosphine; XPhos; In 1,4-dioxane; toluene; 1: |Mitsunobu Displacement;

Reference yield:

: 828-27-3
4-Trifluoromethoxyphenol

: 1418287-68-9
ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate / N,N-dimethyl-formamide / 3 h / 60 °C

2: triethylamine tris(hydrogen fluoride) / acetonitrile / 3 h / 20 °C

3: triphenylphosphine; di-isopropyl azodicarboxylate / toluene / 0 - 20 °C

4: potassium acetate; palladium diacetate; XPhos / 1,4-dioxane / 85 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; potassium acetate; palladium diacetate; caesium carbonate; triethylamine tris(hydrogen fluoride); triphenylphosphine; XPhos; In 1,4-dioxane; N,N-dimethyl-formamide; toluene; acetonitrile; 3: |Mitsunobu Displacement;