Technology Process of Silane,
(1,1-dimethylethyl)[2-[(4S,6S)-6-[[(4R,6R)-6-[[(4R,6S)-6-[[(4R,6R)-6-(2,
2-diphenylethenyl)-2,2-dimethyl-1,3-dioxan-4-yl]methyl]-2,2-dimethyl-1,3
-dioxan-4-yl]methyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]-2,2-dimethyl-1,
3-dioxan-4-yl]ethoxy]dimethyl-
There total 13 articles about Silane,
(1,1-dimethylethyl)[2-[(4S,6S)-6-[[(4R,6R)-6-[[(4R,6S)-6-[[(4R,6R)-6-(2,
2-diphenylethenyl)-2,2-dimethyl-1,3-dioxan-4-yl]methyl]-2,2-dimethyl-1,3
-dioxan-4-yl]methyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]-2,2-dimethyl-1,
3-dioxan-4-yl]ethoxy]dimethyl- 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:
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500533-20-0
tert-Butyl-{2-[(4S,6S)-6-((4R,6R)-6-{(4R,6S)-6-[(4R,6R)-6-(2,2-diphenyl-vinyl)-2,2-dimethyl-[1,3]dioxan-4-ylmethyl]-2,2-dimethyl-[1,3]dioxan-4-ylmethyl}-2,2-dimethyl-[1,3]dioxan-4-ylmethyl)-2,2-dimethyl-[1,3]dioxan-4-yl]-ethoxy}-dimethyl-silane
- Guidance literature:
-
With
Burgess Reagent;
In
toluene;
at 55 ℃;
DOI:10.1055/s-2002-35584
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500533-20-0
tert-Butyl-{2-[(4S,6S)-6-((4R,6R)-6-{(4R,6S)-6-[(4R,6R)-6-(2,2-diphenyl-vinyl)-2,2-dimethyl-[1,3]dioxan-4-ylmethyl]-2,2-dimethyl-[1,3]dioxan-4-ylmethyl}-2,2-dimethyl-[1,3]dioxan-4-ylmethyl)-2,2-dimethyl-[1,3]dioxan-4-yl]-ethoxy}-dimethyl-silane
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: imidazole / dimethylformamide / 0 °C
2.1: NMO; OsO4; H2O / acetone / 20 °C
3.1: aq. NaIO4 / 20 °C
4.1: Bu2BOTf; Et3N / CH2Cl2 / 1 h / -78 - 0 °C
4.2: 65 percent / CH2Cl2; diethyl ether / 6 h / -100 - -78 °C
5.1: 93 percent / (Me4N)BH(OAc)3; AcOH / acetonitrile / -20 °C
6.1: HCOONH4 / Pd/C / methanol / 64 °C
7.1: PPTS / CH2Cl2 / 20 °C
8.1: tetrahydrofuran / 0 °C
9.1: MeO2CNSO2NEt3 / toluene / 55 °C
With
1H-imidazole; sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; Burgess Reagent; di-n-butylboryl trifluoromethanesulfonate; water; ammonium formate; pyridinium p-toluenesulfonate; acetic acid; triethylamine; tetramethylammonium triacetoxyborohydride;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; toluene; acetonitrile;
9.1: Burgess elimination;
DOI:10.1055/s-2002-35584
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-
500533-20-0
tert-Butyl-{2-[(4S,6S)-6-((4R,6R)-6-{(4R,6S)-6-[(4R,6R)-6-(2,2-diphenyl-vinyl)-2,2-dimethyl-[1,3]dioxan-4-ylmethyl]-2,2-dimethyl-[1,3]dioxan-4-ylmethyl}-2,2-dimethyl-[1,3]dioxan-4-ylmethyl)-2,2-dimethyl-[1,3]dioxan-4-yl]-ethoxy}-dimethyl-silane
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: 73 percent / CuCl2*2H2O; H2O; PdCl2 / dimethylformamide / 70 °C
2.1: Bu2BOTf; Et3N / CH2Cl2 / 1 h / -78 - 0 °C
2.2: 65 percent / CH2Cl2; diethyl ether / 6 h / -100 - -78 °C
3.1: 93 percent / (Me4N)BH(OAc)3; AcOH / acetonitrile / -20 °C
4.1: HCOONH4 / Pd/C / methanol / 64 °C
5.1: PPTS / CH2Cl2 / 20 °C
6.1: tetrahydrofuran / 0 °C
7.1: MeO2CNSO2NEt3 / toluene / 55 °C
With
Burgess Reagent; di-n-butylboryl trifluoromethanesulfonate; water; ammonium formate; pyridinium p-toluenesulfonate; acetic acid; triethylamine; palladium dichloride; tetramethylammonium triacetoxyborohydride;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;
1.1: Wacker oxidation / 7.1: Burgess elimination;
DOI:10.1055/s-2002-35584