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(2-hydroxyl-2-phenyl-1-trimethylsilyl-3(Z)-buten-4-yl)(pyridine)bis(dimethylglyoximato)cobalt(III)

Base Information
  • Chemical Name:(2-hydroxyl-2-phenyl-1-trimethylsilyl-3(Z)-buten-4-yl)(pyridine)bis(dimethylglyoximato)cobalt(III)
  • CAS No.:287120-54-1
  • Molecular Formula:C26H38CoN5O5Si
  • Molecular Weight:587.697
  • Hs Code.:
(2-hydroxyl-2-phenyl-1-trimethylsilyl-3(Z)-buten-4-yl)(pyridine)bis(dimethylglyoximato)cobalt(III)

Synonyms:(2-hydroxyl-2-phenyl-1-trimethylsilyl-3(Z)-buten-4-yl)(pyridine)bis(dimethylglyoximato)cobalt(III)

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Chemical Property of (2-hydroxyl-2-phenyl-1-trimethylsilyl-3(Z)-buten-4-yl)(pyridine)bis(dimethylglyoximato)cobalt(III)
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Technology Process of (2-hydroxyl-2-phenyl-1-trimethylsilyl-3(Z)-buten-4-yl)(pyridine)bis(dimethylglyoximato)cobalt(III)

There total 3 articles about (2-hydroxyl-2-phenyl-1-trimethylsilyl-3(Z)-buten-4-yl)(pyridine)bis(dimethylglyoximato)cobalt(III) 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:
Guidance literature:
With NH4Cl; In tetrahydrofuran; under N2, the complex was dissolved in THF, the mixt. was cooled to 0°C, (trimethylsilyl methyl)lithium was slowly added by syringe, thesoln. was warmed to 25°C overnight and poured into an ice/satd. NH4Cl soln.; the mixt. was extd. with CH3CH2OCOCH3, dried (MgSO4), concd. (vac.);
DOI:10.1021/om000230m
Guidance literature:
Multi-step reaction with 2 steps
1: NaBH4; NaOH / methanol
2: NH4Cl / tetrahydrofuran
With NaBH4; NaOH; NH4Cl; In tetrahydrofuran; methanol;
DOI:10.1021/om000230m
Guidance literature:
Multi-step reaction with 2 steps
1: NaBH4; NaOH / methanol
2: NH4Cl / tetrahydrofuran
With NaBH4; NaOH; NH4Cl; In tetrahydrofuran; methanol;
DOI:10.1021/om000230m
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