[((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(CH₃)(HOCH₂CF₃)]⁽¹⁺⁾*BF₄^(1-)=[((CH₃)2C₆H₃NC(CH₃))2Pt(CH₃)(HOCH₂CF₃)]BF₄

Base Information

• Chemical Name: [((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(CH₃)(HOCH₂CF₃)]⁽¹⁺⁾*BF₄^(1-)=[((CH₃)2C₆H₃NC(CH₃))2Pt(CH₃)(HOCH₂CF₃)]BF₄
• CAS No.: 312925-27-2
• Molecular Formula: BF₄*C₂₃H₃₀F₃N₂OPt
• Molecular Weight: 689.384
• Mol file: 312925-27-2.mol

Synonyms:

Chemical Property of [((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(CH₃)(HOCH₂CF₃)]⁽¹⁺⁾*BF₄^(1-)=[((CH₃)2C₆H₃NC(CH₃))2Pt(CH₃)(HOCH₂CF₃)]BF₄

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(CH₃)(HOCH₂CF₃)]⁽¹⁺⁾*BF₄^(1-)=[((CH₃)2C₆H₃NC(CH₃))2Pt(CH₃)(HOCH₂CF₃)]BF₄

There total 2 articles about [((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(CH₃)(HOCH₂CF₃)]⁽¹⁺⁾*BF₄^(1-)=[((CH₃)2C₆H₃NC(CH₃))2Pt(CH₃)(HOCH₂CF₃)]BF₄ 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: 14.0%

tetrafluoroboric acid + 2,2,2-trifluoroethanol (75-89-8) + [2,6-Me2C6H3N=C(Me)C(Me)=N-2,6-Me2C6H3]Pt(Me)(Ph) (312925-38-5) → ((CH3)2C6H3CNCH3)2Pt(C6H5)(HOCH2CF3)(1+) (312925-33-0) + [((CH3)2C6H3NC(CH3)C(CH3)NC6H3(CH3)2)Pt(CH3)(H2O)](1+)*BF4(1-)=[((CH3)2C6H3NC(CH3)C(CH3)NC6H3(CH3)2)Pt(CH3)(H2O)]BF4 (312925-25-0) + [((CH3)2C6H3NC(CH3)C(CH3)NC6H3(CH3)2)Pt(CH3)(HOCH2CF3)](1+)*BF4(1-)=[((CH3)2C6H3NC(CH3))2Pt(CH3)(HOCH2CF3)]BF4 (312925-27-2) + ((CH3)2C6H3CNCH3)2Pt(H2O)(C6H5)(1+)*BF4(1-)=((CH3)2C6H3CNCH3)2PtC6H5(H2O)BF4 (312925-32-9)

Guidance literature:

With water; In further solvent(s); byproducts: CH4; to an NMR tube loaded with complex was added a 48% aq. HBF4 dissolve intrifluoroethanol, 25°C; not sepd., detected by NMR spectra;

DOI:10.1021/ja0017460

Reference yield:

2,2,2-trifluoroethanol (75-89-8) + [((CH3)2C6H3NC(CH3)C(CH3)NC6H3(CH3)2)Pt(CH3)(H2O)](1+)*BF4(1-)=[((CH3)2C6H3NC(CH3)C(CH3)NC6H3(CH3)2)Pt(CH3)(H2O)]BF4 (312925-25-0) → [((CH3)2C6H3NC(CH3)C(CH3)NC6H3(CH3)2)Pt(CH3)(HOCH2CF3)](1+)*BF4(1-)=[((CH3)2C6H3NC(CH3))2Pt(CH3)(HOCH2CF3)]BF4 (312925-27-2)

Guidance literature:

In further solvent(s); Pt complex in trifluroethanol; not isolated;

Reference yield:

[((CH3)2C6H3NC(CH3)C(CH3)NC6H3(CH3)2)Pt(CH3)(HOCH2CF3)](1+)*BF4(1-)=[((CH3)2C6H3NC(CH3))2Pt(CH3)(HOCH2CF3)]BF4 (312925-27-2) + benzene (71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1) → [((CH3)2C6H3NC(CH3)C(CH3)NC6H3(CH3)2)Pt(C6H5)(HOCH2CF3)](1+)*BF4(1-)=[((CH3)2C6H3NC(CH3))2Pt(C6H5)(HOCH2CF3)]BF4 (312925-34-1)

Guidance literature:

In water; byproducts: CH4; Pt complex in trifluoroethanol/H2O was reacted with benzene at 25-45°C; not isolated; Kinetics;

upstream raw materials:

2,2,2-trifluoroethanol

[2,6-Me₂C₆H₃N=C(Me)C(Me)=N-2,6-Me₂C₆H₃]Pt(Me)(Ph)

[((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(CH₃)(H₂O)]⁽¹⁺⁾*BF₄^(1-)=[((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(CH₃)(H₂O)]BF₄

Downstream raw materials:

[((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(CH₃)(H₂O)]⁽¹⁺⁾*BF₄^(1-)=[((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(CH₃)(H₂O)]BF₄

[((CH₃)2C₆H₃NC(CH₃)C(CH₃)NC₆H₃(CH₃)2)Pt(C₆H₅)(HOCH₂CF₃)]⁽¹⁺⁾*BF₄^(1-)=[((CH₃)2C₆H₃NC(CH₃))2Pt(C₆H₅)(HOCH₂CF₃)]BF₄