C₃₀H₂₄BClF₂N₂O₃S

Base Information Edit

Chemical Name:C₃₀H₂₄BClF₂N₂O₃S
CAS No.:1620546-01-1
Molecular Formula:C₃₀H₂₄BClF₂N₂O₃S
Molecular Weight:576.859
Hs Code.:
Mol file:1620546-01-1.mol

C<sub>30</sub>H<sub>24</sub>BClF<sub>2</sub>N<sub>2</sub>O<sub>3</sub>S

Synonyms:C₃₀H₂₄BClF₂N₂O₃S

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Chemical Property of C₃₀H₂₄BClF₂N₂O₃S Edit

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Technology Process of C₃₀H₂₄BClF₂N₂O₃S

There total 7 articles about C₃₀H₂₄BClF₂N₂O₃S 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: 61.0%

: 1620546-00-0
C₂₄H₁₂BrClF₂N₂OS

: 73183-34-3
bis(pinacol)diborane

: 1620546-01-1
C₃₀H₂₄BClF₂N₂O₃S

Guidance literature:: With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In 1,4-dioxane; at 110 ℃; for 2h; Inert atmosphere;

Reference yield:

: 1765-93-1
4-fluoroboronic acid

: 1620546-01-1
C₃₀H₂₄BClF₂N₂O₃S

Guidance literature:: Multi-step reaction with 5 steps

1.1: catacxium A; palladium diacetate; caesium carbonate / water; toluene / 16 h / 100 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran / 2 h / -78 °C / Inert atmosphere

2.2: 1 h / -78 - 25 °C

3.1: trifluoroacetic acid / acetonitrile / 1 h / 25 °C

4.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / toluene / 3 h / Reflux

5.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate / 1,4-dioxane / 2 h / 110 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; n-butyllithium; potassium acetate; palladium diacetate; caesium carbonate; trifluoroacetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; catacxium A; In tetrahydrofuran; 1,4-dioxane; water; toluene; acetonitrile;

Reference yield:

: 1005196-13-3
2-(4-fluorophenyl)thiazole

: 1620546-01-1
C₃₀H₂₄BClF₂N₂O₃S

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / tetrahydrofuran / 2 h / -78 °C / Inert atmosphere

1.2: 1 h / -78 - 25 °C

2.1: trifluoroacetic acid / acetonitrile / 1 h / 25 °C

3.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / toluene / 3 h / Reflux

4.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate / 1,4-dioxane / 2 h / 110 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; n-butyllithium; potassium acetate; trifluoroacetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; 1,4-dioxane; toluene; acetonitrile;