2-(2-((4-methoxybenzyl)oxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Base Information

Chemical Name:2-(2-((4-methoxybenzyl)oxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS No.:935846-39-2
Molecular Formula:C₂₀H₂₅BO₄
Molecular Weight:340.227
Hs Code.:

Synonyms:2-(2-((4-methoxybenzyl)oxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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Chemical Property of 2-(2-((4-methoxybenzyl)oxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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Technology Process of 2-(2-((4-methoxybenzyl)oxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

There total 6 articles about 2-(2-((4-methoxybenzyl)oxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 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: 82.0%

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

: 637301-05-4
4-methoxybenzyl 2’-iodophenyl ether

: 935846-39-2
2-(2-((4-methoxybenzyl)oxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Guidance literature:: With triethylamine; CyJohnPhos; palladium diacetate; In 1,4-dioxane; at 85 ℃; for 0.166667h;
DOI:10.1021/jo062627r

Reference yield: 60.0%

: 1-bromo-2-((4-methoxybenzyl)oxy)benzene

: 73183-34-3
bis(pinacol)diborane

: 935846-39-2
2-(2-((4-methoxybenzyl)oxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Guidance literature:: With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In 1,4-dioxane; for 18h; Inert atmosphere; Reflux;

Reference yield:

: 533-58-4
2-Iodophenol

: 935846-39-2
2-(2-((4-methoxybenzyl)oxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / potassium carbonate; tetra-n-butylammonium iodide; 18-crown-6 / acetone / Heating

2: 82 percent / triethylamine; 2-(dicyclohexylphosphino)biphenyl / palladium(II) acetate / dioxane / 0.17 h / 85 °C

With 18-crown-6 ether; tetra-(n-butyl)ammonium iodide; potassium carbonate; triethylamine; CyJohnPhos; palladium diacetate; In 1,4-dioxane; acetone;
DOI:10.1021/jo062627r