((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄B(neopentyl glycolato)

Base Information

Chemical Name:((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄B(neopentyl glycolato)
CAS No.:1164223-68-0
Molecular Formula:C₇₂H₇₉BN₂O₆
Molecular Weight:1079.24
Hs Code.:

((CH<sub>3</sub>)3CC<sub>6</sub>H<sub>4</sub>)3CC<sub>6</sub>H<sub>4</sub>O(CH<sub>2</sub>CH<sub>2</sub>O)3C<sub>6</sub>H<sub>4</sub>C<sub>12</sub>H<sub>6</sub>N<sub>2</sub>C<sub>6</sub>H<sub>4</sub>B(neopentyl glycolato)

Synonyms:((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄B(neopentyl glycolato)

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Chemical Property of ((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄B(neopentyl glycolato)

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Technology Process of ((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄B(neopentyl glycolato)

There total 11 articles about ((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄B(neopentyl glycolato) 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: 100.0%

: 1164223-66-8
((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄Br

: 2-(2,2-dimethyl-1,3,5-dioxaborinan-5-yl)-5,5-dimethyl-1,3,2-dioxaborinane

: 1164223-68-0
((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄B(neopentyl glycolato)

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; In 1,4-dioxane; at 80 ℃; Inert atmosphere;
DOI:10.1002/anie.200903311

Reference yield: 100.0%

: 1164223-66-8
((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄Br

: 201733-56-4
2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-5,5-dimethyl-1,3,2-dioxaborinane

: 1164223-68-0
((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄B(neopentyl glycolato)

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; In 1,4-dioxane; at 80 ℃; for 16h; Inert atmosphere;
DOI:10.1039/b9nj00296k

Reference yield:

: 351523-94-9
2-[2-[2-[4-[tris[4-(tert-butyl)phenyl]methyl]phenoxy]ethoxy]ethoxy]ethanol

: 1164223-68-0
((CH₃)3CC₆H₄)3CC₆H₄O(CH₂CH₂O)3C₆H₄C₁₂H₆N₂C₆H₄B(neopentyl glycolato)

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 4 h / 0 °C

2: sodium iodide / acetone / 16 h / Inert atmosphere

3: caesium carbonate / N,N-dimethyl-formamide / 16 h / 50 °C

4: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; caesium carbonate; triethylamine; sodium iodide; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; acetone; 3: Williamson synthesis;
DOI:10.1039/b9nj00296k