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C35H48O8Si

Base Information
  • Chemical Name:C35H48O8Si
  • CAS No.:214484-10-3
  • Molecular Formula:C35H48O8Si
  • Molecular Weight:624.847
  • Hs Code.:
C<sub>35</sub>H<sub>48</sub>O<sub>8</sub>Si

Synonyms:C35H48O8Si

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Chemical Property of C35H48O8Si
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Technology Process of C35H48O8Si

There total 15 articles about C35H48O8Si 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 pyridine; dmap; In dichloromethane; at 20 ℃; for 16h;
DOI:10.1016/S0040-4020(02)00050-9
Guidance literature:
Multi-step reaction with 11 steps
1.1: AD-mix-α / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C
2.1: CSA / benzene; methanol / 32 h
2.2: H2 / Pd(OH)2 / ethanol / 12 h / 20 °C / 760 Torr
3.1: 98 percent / TFA / methanol / 0.83 h / Heating
4.1: 75 percent / NMO; 4 Angstroem molecular sieves; TPAP / 2-methyl-propan-2-ol; acetonitrile / 20 °C
5.1: pyridine / tetrahydrofuran; toluene / 0.75 h / -78 - 20 °C
5.2: 9-BBN / tetrahydrofuran; toluene / 0.5 h / 20 °C
5.3: 40 percent / NaBO3*4H2O / tetrahydrofuran; toluene / 2 h
6.1: Dess-Martin periodinane reagent / CH2Cl2 / 2.5 h / 20 °C
7.1: 77 percent / TiCl4 / CH2Cl2 / 0.33 h / -78 °C
8.1: 91 percent / pyridine; DMAP / 27 h / 20 °C
9.1: 99 percent / IBr / toluene; CH2Cl2 / 3 h / -80 °C
10.1: 90 percent / aq. LiOH / 1,2-dimethoxy-ethane / 13 h / 60 °C
11.1: 90 percent / pyridine; DMAP / CH2Cl2 / 16 h / 20 °C
With pyridine; dmap; lithium hydroxide; AD-mix-α; N-methyl-2-indolinone; tetrapropylammonium perruthennate; 4 A molecular sieve; camphor-10-sulfonic acid; iodine(I) bromide; titanium tetrachloride; Dess-Martin periodane; trifluoroacetic acid; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; water; toluene; acetonitrile; tert-butyl alcohol; benzene;
DOI:10.1016/S0040-4020(02)00050-9
Guidance literature:
Multi-step reaction with 13 steps
1.1: 84 percent / HMDS; TMEDA; n-BuLi / tetrahydrofuran / 0 °C
2.1: 96 percent / aq. LiCl / dimethylsulfoxide / 0.67 h / 190 °C
3.1: AD-mix-α / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C
4.1: CSA / benzene; methanol / 32 h
4.2: H2 / Pd(OH)2 / ethanol / 12 h / 20 °C / 760 Torr
5.1: 98 percent / TFA / methanol / 0.83 h / Heating
6.1: 75 percent / NMO; 4 Angstroem molecular sieves; TPAP / 2-methyl-propan-2-ol; acetonitrile / 20 °C
7.1: pyridine / tetrahydrofuran; toluene / 0.75 h / -78 - 20 °C
7.2: 9-BBN / tetrahydrofuran; toluene / 0.5 h / 20 °C
7.3: 40 percent / NaBO3*4H2O / tetrahydrofuran; toluene / 2 h
8.1: Dess-Martin periodinane reagent / CH2Cl2 / 2.5 h / 20 °C
9.1: 77 percent / TiCl4 / CH2Cl2 / 0.33 h / -78 °C
10.1: 91 percent / pyridine; DMAP / 27 h / 20 °C
11.1: 99 percent / IBr / toluene; CH2Cl2 / 3 h / -80 °C
12.1: 90 percent / aq. LiOH / 1,2-dimethoxy-ethane / 13 h / 60 °C
13.1: 90 percent / pyridine; DMAP / CH2Cl2 / 16 h / 20 °C
With pyridine; dmap; lithium hydroxide; AD-mix-α; n-butyllithium; N-methyl-2-indolinone; tetrapropylammonium perruthennate; N,N,N,N,-tetramethylethylenediamine; 4 A molecular sieve; camphor-10-sulfonic acid; iodine(I) bromide; titanium tetrachloride; Dess-Martin periodane; 1,1,1,3,3,3-hexamethyl-disilazane; trifluoroacetic acid; lithium chloride; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; water; dimethyl sulfoxide; toluene; acetonitrile; tert-butyl alcohol; benzene;
DOI:10.1016/S0040-4020(02)00050-9
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