C₃₉H₃₁BF₂N₂

Base Information

Chemical Name:C₃₉H₃₁BF₂N₂
CAS No.:1303477-84-0
Molecular Formula:C₃₉H₃₁BF₂N₂
Molecular Weight:576.496
Hs Code.:

C<sub>39</sub>H<sub>31</sub>BF<sub>2</sub>N<sub>2</sub>

Synonyms:C₃₉H₃₁BF₂N₂

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Chemical Property of C₃₉H₃₁BF₂N₂

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Technology Process of C₃₉H₃₁BF₂N₂

There total 6 articles about C₃₉H₃₁BF₂N₂ 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: 99.0%

: C₃₉H₃₂N₂

: 1303477-84-0
C₃₉H₃₁BF₂N₂

Guidance literature:: With boron trifluoride diethyl etherate; N-ethyl-N,N-diisopropylamine; In toluene; at 20 ℃; for 0.5h;
DOI:10.1016/j.tet.2011.03.016

Reference yield:

: C₂₄H₂₇NO₄

: 1303477-84-0
C₃₉H₃₁BF₂N₂

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide / ethylene glycol / 2 h / 175 °C / Inert atmosphere; Darkness

2.1: trifluoroacetic acid / dichloromethane / Reflux; Inert atmosphere

2.2: 20 °C / Inert atmosphere

3.1: boron trifluoride diethyl etherate; N-ethyl-N,N-diisopropylamine / toluene / 0.5 h / 20 °C

With boron trifluoride diethyl etherate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; potassium hydroxide; In dichloromethane; ethylene glycol; toluene;
DOI:10.1016/j.tet.2011.03.016

Reference yield:

: 1303477-70-4
C₁₆H₁₅N

: 1303477-84-0
C₃₉H₃₁BF₂N₂

Guidance literature:: Multi-step reaction with 2 steps

1.1: trifluoroacetic acid / dichloromethane / Reflux; Inert atmosphere

1.2: 20 °C / Inert atmosphere

2.1: boron trifluoride diethyl etherate; N-ethyl-N,N-diisopropylamine / toluene / 0.5 h / 20 °C

With boron trifluoride diethyl etherate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; toluene;
DOI:10.1016/j.tet.2011.03.016