C₃₆H₄₅B₂NO₆

Base Information

Chemical Name:C₃₆H₄₅B₂NO₆
CAS No.:1449490-10-1
Molecular Formula:C₃₆H₄₅B₂NO₆
Molecular Weight:609.378
Hs Code.:

C<sub>36</sub>H<sub>45</sub>B<sub>2</sub>NO<sub>6</sub>

Synonyms:C₃₆H₄₅B₂NO₆

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Chemical Property of C₃₆H₄₅B₂NO₆

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Technology Process of C₃₆H₄₅B₂NO₆

There total 3 articles about C₃₆H₄₅B₂NO₆ 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: 89.0%

: 1449490-09-8
C₂₄H₂₁Br₂NO₂

: 73183-34-3
bis(pinacol)diborane

: 1449490-10-1
C₃₆H₄₅B₂NO₆

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; In 1,4-dioxane; at 80 ℃; for 3h;
DOI:10.1016/j.tetlet.2013.07.025

Reference yield:

: 81-84-5
1,8-Naphthalic anhydride

: 1449490-10-1
C₃₆H₄₅B₂NO₆

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-Bromosuccinimide; sulfuric acid / 6 h / 60 °C

2.1: acetic acid / 4 h / Reflux

2.2: 4 h / Reflux

3.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate / 1,4-dioxane / 3 h / 80 °C

With N-Bromosuccinimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; sulfuric acid; potassium acetate; acetic acid; In 1,4-dioxane;
DOI:10.1016/j.tetlet.2013.07.025

Reference yield:

: 1190615-88-3
C₁₂H₄Br₂O₃

: 1449490-10-1
C₃₆H₄₅B₂NO₆

Guidance literature:: Multi-step reaction with 2 steps

1.1: acetic acid / 4 h / Reflux

1.2: 4 h / Reflux

2.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate / 1,4-dioxane / 3 h / 80 °C

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; acetic acid; In 1,4-dioxane;
DOI:10.1016/j.tetlet.2013.07.025