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2-benzylidene-3-oxo-5-phenyl-2,3-dihydrotellurophene

Base Information
  • Chemical Name:2-benzylidene-3-oxo-5-phenyl-2,3-dihydrotellurophene
  • CAS No.:81028-19-5
  • Molecular Formula:C17H12OTe
  • Molecular Weight:359.882
  • Hs Code.:
2-benzylidene-3-oxo-5-phenyl-2,3-dihydrotellurophene

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Chemical Property of 2-benzylidene-3-oxo-5-phenyl-2,3-dihydrotellurophene
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Technology Process of 2-benzylidene-3-oxo-5-phenyl-2,3-dihydrotellurophene

There total 3 articles about 2-benzylidene-3-oxo-5-phenyl-2,3-dihydrotellurophene 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 tetrabutyl ammonium fluoride; 1,3-di-tert-butyl-1,1,3,3-tetramethyldisilatellurane; In tert-butyl alcohol; for 1h; Ambient temperature;
DOI:10.1021/jo00349a030
Guidance literature:
Multi-step reaction with 2 steps
1: 72 percent / Na2Cr2O7 in aq. H2SO4 / acetone
2: 28 percent / bis((tert-butyldimethylsilyl) telluride, tetra-n-butylammonium fluoride / 2-methyl-propan-2-ol / 1 h / Ambient temperature
With sodium dichromate; sulfuric acid; tetrabutyl ammonium fluoride; 1,3-di-tert-butyl-1,1,3,3-tetramethyldisilatellurane; In acetone; tert-butyl alcohol;
DOI:10.1021/jo00349a030
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) EtBr, Mg, I2 / 1.) ether, RT, 3 h
2: 72 percent / Na2Cr2O7 in aq. H2SO4 / acetone
3: 28 percent / bis((tert-butyldimethylsilyl) telluride, tetra-n-butylammonium fluoride / 2-methyl-propan-2-ol / 1 h / Ambient temperature
With sodium dichromate; sulfuric acid; tetrabutyl ammonium fluoride; iodine; ethidium Bromide; 1,3-di-tert-butyl-1,1,3,3-tetramethyldisilatellurane; magnesium; In acetone; tert-butyl alcohol;
DOI:10.1021/jo00349a030
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