C₃₀H₃₃FN₂O₂

Base Information

Chemical Name:C₃₀H₃₃FN₂O₂
CAS No.:1597602-47-5
Molecular Formula:C₃₀H₃₃FN₂O₂
Molecular Weight:472.603
Hs Code.:

C<sub>30</sub>H<sub>33</sub>FN<sub>2</sub>O<sub>2</sub>

Synonyms:C₃₀H₃₃FN₂O₂

Suppliers and Price of C₃₀H₃₃FN₂O₂

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₃₀H₃₃FN₂O₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₀H₃₃FN₂O₂

There total 6 articles about C₃₀H₃₃FN₂O₂ 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:

: 58164-14-0
1-bromo-2-amino-4-tert-butylbenzene

: 1597602-47-5
C₃₀H₃₃FN₂O₂

Guidance literature:: Multi-step reaction with 4 steps

1.1: nitrosonium tetrafluoroborate / dichloromethane / 13.5 h / 0 - 20 °C / Inert atmosphere

1.2: 2 h / Inert atmosphere; Reflux

2.1: n-butyllithium / tetrahydrofuran / 2.33 h / -77 °C

2.2: 14.17 h / -77 - 20 °C

2.3: 55 h

3.1: [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; N-ethyl-N,N-diisopropylamine / ethanol / 4 h / Inert atmosphere; Reflux

4.1: titanium tetrachloride / toluene / 20.08 h / 0 - 20 °C / Inert atmosphere

With n-butyllithium; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; titanium tetrachloride; nitrosonium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; dichloromethane; toluene; 1.1: |Balz-Schiemann Reaction / 3.1: |Suzuki-Miyaura Coupling;
DOI:10.1002/chem.201304241

Reference yield:

: 1369829-80-0
1-bromo-2-fluoro-4-tertbutylbenzene

: 1597602-47-5
C₃₀H₃₃FN₂O₂

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran / 2.33 h / -77 °C

1.2: 14.17 h / -77 - 20 °C

1.3: 55 h

2.1: [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; N-ethyl-N,N-diisopropylamine / ethanol / 4 h / Inert atmosphere; Reflux

3.1: titanium tetrachloride / toluene / 20.08 h / 0 - 20 °C / Inert atmosphere

With n-butyllithium; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; titanium tetrachloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; toluene; 2.1: |Suzuki-Miyaura Coupling;
DOI:10.1002/chem.201304241

Reference yield:

: 70729-05-4
1-Bromo-4-tert-butyl-2-nitro-benzene

: 1597602-47-5
C₃₀H₃₃FN₂O₂

Guidance literature:: Multi-step reaction with 5 steps

1.1: iron / acetic acid; ethanol / 2 h / 100 °C / Inert atmosphere

2.1: nitrosonium tetrafluoroborate / dichloromethane / 13.5 h / 0 - 20 °C / Inert atmosphere

2.2: 2 h / Inert atmosphere; Reflux

3.1: n-butyllithium / tetrahydrofuran / 2.33 h / -77 °C

3.2: 14.17 h / -77 - 20 °C

3.3: 55 h

4.1: [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; N-ethyl-N,N-diisopropylamine / ethanol / 4 h / Inert atmosphere; Reflux

5.1: titanium tetrachloride / toluene / 20.08 h / 0 - 20 °C / Inert atmosphere

With n-butyllithium; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; titanium tetrachloride; iron; nitrosonium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; dichloromethane; acetic acid; toluene; 2.1: |Balz-Schiemann Reaction / 4.1: |Suzuki-Miyaura Coupling;
DOI:10.1002/chem.201304241