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(Z)-(2-(benzhydryloxy)-1-(2,5-dimethoxyphenyl)ethenyloxy)trimethyl silane

Base Information
  • Chemical Name:(Z)-(2-(benzhydryloxy)-1-(2,5-dimethoxyphenyl)ethenyloxy)trimethyl silane
  • CAS No.:866416-81-1
  • Molecular Formula:C26H30O4Si
  • Molecular Weight:434.607
  • Hs Code.:
(Z)-(2-(benzhydryloxy)-1-(2,5-dimethoxyphenyl)ethenyloxy)trimethyl silane

Synonyms:(Z)-(2-(benzhydryloxy)-1-(2,5-dimethoxyphenyl)ethenyloxy)trimethyl silane

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Chemical Property of (Z)-(2-(benzhydryloxy)-1-(2,5-dimethoxyphenyl)ethenyloxy)trimethyl silane
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Technology Process of (Z)-(2-(benzhydryloxy)-1-(2,5-dimethoxyphenyl)ethenyloxy)trimethyl silane

There total 1 articles about (Z)-(2-(benzhydryloxy)-1-(2,5-dimethoxyphenyl)ethenyloxy)trimethyl silane 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:
2-(benzhydryloxy)-1-(2,5-dimethoxyphenyl)-ethanone; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 1h;
chloro-trimethyl-silane; In tetrahydrofuran; at -78 - 20 ℃;
DOI:10.1021/ol051096a
Guidance literature:
Multi-step reaction with 4 steps
1: O(9)-allyl-N-2',3',4'-trifluorobenzylhydrocinchonium*HF2(1-) / tetrahydrofuran / 24 h / -55 °C
2: 97 percent / pyridine; DMAP / ethyl acetate / 0 - 20 °C
3: 77 percent / titanium(IV) chloride / CH2Cl2 / 2 h / -78 °C
4: 79 percent / K2CO3; tin tetrachloride; bis(trimethylsilyl) peroxide / molecular sieves 4 Angstroem; trans-N,N-bis(p-toluenesulfonyl)-1,2-cyclohexanediamine / CH2Cl2 / 0.83 h / 0 °C
With pyridine; dmap; bis-trimethylsilanyl peroxide; O(9)-allyl-N-2',3',4'-trifluorobenzylhydrocinchonium*HF2(1-); titanium tetrachloride; tin(IV) chloride; potassium carbonate; 4 A molecular sieve; trans-N,N-bis(p-toluenesulfonyl)-1,2-cyclohexanediamine; In tetrahydrofuran; dichloromethane; ethyl acetate; 4: Baeyer-Villiger reaction;
DOI:10.1021/ol051096a
Guidance literature:
Multi-step reaction with 5 steps
1: O(9)-allyl-N-2',3',4'-trifluorobenzylhydrocinchonium*HF2(1-) / tetrahydrofuran / 24 h / -55 °C
2: 97 percent / pyridine; DMAP / ethyl acetate / 0 - 20 °C
3: 77 percent / titanium(IV) chloride / CH2Cl2 / 2 h / -78 °C
4: 79 percent / K2CO3; tin tetrachloride; bis(trimethylsilyl) peroxide / molecular sieves 4 Angstroem; trans-N,N-bis(p-toluenesulfonyl)-1,2-cyclohexanediamine / CH2Cl2 / 0.83 h / 0 °C
5: 85 percent / NaOMe / tetrahydrofuran / 0 - 20 °C
With pyridine; dmap; bis-trimethylsilanyl peroxide; O(9)-allyl-N-2',3',4'-trifluorobenzylhydrocinchonium*HF2(1-); sodium methylate; titanium tetrachloride; tin(IV) chloride; potassium carbonate; 4 A molecular sieve; trans-N,N-bis(p-toluenesulfonyl)-1,2-cyclohexanediamine; In tetrahydrofuran; dichloromethane; ethyl acetate; 4: Baeyer-Villiger reaction;
DOI:10.1021/ol051096a
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