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Technology Process of [Ti(C3H7N(CH2C6H2(C(CH3)3)2O)2)(C5H5N)(NC6H3(CH(CH3)2)2)]

[Ti(C3H7N(CH2C6H2(C(CH3)3)2O)2)(C5H5N)(NC6H3(CH(CH3)2)2)]

Base Information
  • Chemical Name:[Ti(C3H7N(CH2C6H2(C(CH3)3)2O)2)(C5H5N)(NC6H3(CH(CH3)2)2)]
  • CAS No.:837429-65-9
  • Molecular Formula:C50H73N3O2Ti
  • Molecular Weight:796.029
  • Hs Code.:
[Ti(C<sub>3</sub>H<sub>7</sub>N(CH<sub>2</sub>C<sub>6</sub>H<sub>2</sub>(C(CH<sub>3</sub>)3)2O)2)(C<sub>5</sub>H<sub>5</sub>N)(NC<sub>6</sub>H<sub>3</sub>(CH(CH<sub>3</sub>)2)2)]

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Chemical Property of [Ti(C3H7N(CH2C6H2(C(CH3)3)2O)2)(C5H5N)(NC6H3(CH(CH3)2)2)]
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Technology Process of [Ti(C3H7N(CH2C6H2(C(CH3)3)2O)2)(C5H5N)(NC6H3(CH(CH3)2)2)]

There total 1 articles about [Ti(C3H7N(CH2C6H2(C(CH3)3)2O)2)(C5H5N)(NC6H3(CH(CH3)2)2)] 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: 21.0%

[Ti(N-2,6-C<sub>6</sub>H<sub>3</sub>Pr(i)2)Cl<sub>2</sub>(pyridine)3]

[Ti(N-2,6-C6H3Pr(i)2)Cl2(pyridine)3]

Na<sub>2</sub>(PrN(CH<sub>2</sub>-2-O-3,5-C<sub>6</sub>H<sub>2</sub>(t-Bu)2)2)

Na2(PrN(CH2-2-O-3,5-C6H2(t-Bu)2)2)

[Ti(C<sub>3</sub>H<sub>7</sub>N(CH<sub>2</sub>C<sub>6</sub>H<sub>2</sub>(C(CH<sub>3</sub>)3)2O)2)(C<sub>5</sub>H<sub>5</sub>N)(NC<sub>6</sub>H<sub>3</sub>(CH(CH<sub>3</sub>)2)2)]
836659-26-8,837429-65-9

[Ti(C3H7N(CH2C6H2(C(CH3)3)2O)2)(C5H5N)(NC6H3(CH(CH3)2)2)]

Guidance literature:
In tetrahydrofuran; inert atm.; soln. of Na salt in THF added to soln. of Ti complex in THF under stirring, heated at 60°C for 16 h, allowed to cool to room temp.; volatiles removed under reduced pressure, residue extd. with pentane/CH2Cl2 (9/1), extract stored at -80°C, ppt. sepd., washed with cold pentane (-80°C), dried under vac.;
DOI:10.1021/om0493661
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