Alternatived Products of [ 16415-13-7 ]
Product Details of [ 16415-13-7 ]
CAS No. : | 16415-13-7 |
MDL No. : | MFCD00054793 |
Formula : |
C22H48O3Si
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | OYGYKEULCAINCL-UHFFFAOYSA-N |
M.W : |
388.70
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Pubchem ID : | 85407 |
Synonyms : |
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Application In Synthesis of [ 16415-13-7 ]
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
- Downstream synthetic route of [ 16415-13-7 ]
- 1
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[ 16415-13-7 ]
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[ 408-21-9 ]
Yield | Reaction Conditions | Operation in experiment |
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With hydrogen fluoride; water |
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With HF In hydrogen fluoride aq. HF; |
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- 2
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[ 998-30-1 ]
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[ 629-73-2 ]
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[ 16415-13-7 ]
Yield | Reaction Conditions | Operation in experiment |
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for 46h; Heating; |
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100 %Chromat. |
With hydridochlorotris(triphenylphosphine)ruthenium(II); tris(dibutylamino)(dioctylamino)phosphonium hexafluorophosphate at 95℃; for 2h; |
|
76 %Spectr. |
With [Rh(OH)cod]2 and diethylaminopropyltrimethoxysilane immobilized on SiO2 In neat (no solvent) at 40℃; for 0.5h; |
|
Reference:
[1]Hosomi, Akira; Iijima, Susumu; Sakurai, Hideki
[Chemistry Letters, 1981, p. 243 - 246]
[2]Location in patent: experimental part
Wang, Diliang; Li, Jiayun; Peng, Jiajian; Bai, Ying; Lai, Guoqiao
[Phosphorus, Sulfur and Silicon and the Related Elements, 2011, vol. 186, # 11, p. 2258 - 2266]
[3]Motokura, Ken; Maeda, Kyogo; Chun, Wang-Jae
[ACS Catalysis, 2017, vol. 7, # 7, p. 4637 - 4641]
- 3
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[ 16415-13-7 ]
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[ 36653-82-4 ]
Yield | Reaction Conditions | Operation in experiment |
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With disodium hydrogenphosphate; water; 3-chloro-benzenecarboperoxoic acid 1.) methanol, RT, 24 h; Yield given. Multistep reaction; |
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Yield | Reaction Conditions | Operation in experiment |
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Trichlorhexadecylsilan, Ethanol; |
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Trichlor-hexadecyl-silan, EtOH; |
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With particular preference, the alkoxysilanes set out below are prepared by the process of the invention: ... octyltriethoxysilane, cyclohexyltrimethoxysilane, cyclohexylmethyldimethoxysilane, hexadecyltrimethoxysilane, hexadecyltriethoxysilane. |
- 5
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[ 16415-13-7 ]
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[ 171194-90-4 ]
Yield | Reaction Conditions | Operation in experiment |
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With water |
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With hydrogenchloride In ethanol for 7h; |
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Reference:
[1]Shimojima, Atsushi; Kuroda, Kazuyuki
[Angewandte Chemie - International Edition, 2003, vol. 42, # 34, p. 4057 - 4060]
[2]Shimojima, Atsushi; Liu, Zheng; Ohsuna, Tetsu; Terasaki, Osamu; Kuroda, Kazuyuki
[Journal of the American Chemical Society, 2005, vol. 127, # 40, p. 14108 - 14116]
- 6
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[ 64-17-5 ]
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[ 5894-60-0 ]
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[ 16415-13-7 ]
- 7
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[ 16415-13-7 ]
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C16H33Cl7O2Si3
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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Multi-step reaction with 2 steps
1: H2O
2: tetrachlorosilane / tetrahydrofuran; hexane / 20 °C |
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- 8
-
[ 16415-13-7 ]
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C16H33Cl9O3Si4
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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Multi-step reaction with 2 steps
1: H2O
2: tetrachlorosilane / tetrahydrofuran; hexane / 20 °C |
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- 9
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POM-7
[ No CAS ]
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[ 66-40-0 ]
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[ 16415-13-7 ]
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[tetraethylammonium]3[PW11O39(Si(CH2)15CH3)2]
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With HCl In not given treatment of tungstate deriv. with silicate deriv. in presence of tetraethylammonium ions; elem. anal.; |
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- 10
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POM-7
[ No CAS ]
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[ 10549-76-5 ]
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[ 16415-13-7 ]
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[Bu4N]3[PW11O39(Si(CH2)15CH3)2]
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With HCl In not given treatment of tungstate deriv. with silicate deriv. in presence of tetrabutylammonium ions; elem. anal.; |
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- 11
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[ 60-12-8 ]
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[ 16415-13-7 ]
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[ 1185275-68-6 ]
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hexadecylsilicic acid bis(2-phenylethyl) ethyl ester
[ No CAS ]
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C64H102O5Si2
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With sodium methylate In methanol at 113 - 120℃; for 5h; Inert atmosphere; |
3 Preparation Example 3 Preparation of a functional substance-releasing agent containing hexadecylsilicic acid tris (2-phenylethyl)ester[tris (2-phenylethyloxy)hexadecylsilane]
In a 200 mL four-neck flask, under nitrogen flow, 50.56 g of hexadecyltriethoxysilane (0.13 mol), 44.43 g of 2-phenylethanol (0.36 mol), and 0.375 mL of 2.8% sodium methoxide in methanol were stirred for two hours at 113 to 120° C. with distilling off ethanol. After two hours, an inner pressure of the flask was gradually reduced to 8 kPa, and the mixture was stirred for additional three hours at 120° C. with distilling off ethanol. After three hours, the mixture was cooled and the reduced pressure was released. Then, the mixture was filtered to give 77.52 g of yellow oil containing hexadecylsilicic acid tris(2-phenylethyl)ester. The resultant oil was analyzed by GC. The result is shown in Table 3. From the result, contents of hexadecylsilicic acid tris(2-phenylethyl)ester of the compound (1) and hexadecylsilicic acid bis(2-phenylethyl)ethyl ester of the compound (2) were 69.9% and 19.9%, respectively. |