C₇₃H₁₁₈O₁₆Si₂

Base Information

Chemical Name:C₇₃H₁₁₈O₁₆Si₂
CAS No.:329359-65-1
Molecular Formula:C₇₃H₁₁₈O₁₆Si₂
Molecular Weight:1307.9
Hs Code.:

C<sub>73</sub>H<sub>118</sub>O<sub>16</sub>Si<sub>2</sub>

Synonyms:C₇₃H₁₁₈O₁₆Si₂

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Chemical Property of C₇₃H₁₁₈O₁₆Si₂

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Technology Process of C₇₃H₁₁₈O₁₆Si₂

There total 1 articles about C₇₃H₁₁₈O₁₆Si₂ 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:

Reference yield: 91.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 329359-64-0
C₆₁H₉₀O₁₆

: 329359-65-1
C₇₃H₁₁₈O₁₆Si₂

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide;
DOI:10.1002/1521-3773(20010105)40:1<191::AID-ANIE191>3.0.CO;2-C

Reference yield: 82.0%

: 329359-65-1
C₇₃H₁₁₈O₁₆Si₂

: 329359-50-4
C₆₉H₁₁₀O₁₅Si₂

Guidance literature:: With perchloric acid; In dichloromethane;
DOI:10.1002/1521-3773(20010105)40:1<191::AID-ANIE191>3.0.CO;2-C

Reference yield:

: 329359-65-1
C₇₃H₁₁₈O₁₆Si₂

: 204448-45-3
C₄₆H₇₀O₁₆

Guidance literature:: Multi-step reaction with 7 steps

1: 82 percent / aq. HClO₄ / CH₂Cl₂

2: 95 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinine / CH₂Cl₂; H₂O / 0 °C

3: 96 percent / DMAP; pyridine / tetrahydrofuran

4: 100 percent / 1-methyl-1,4-cyclohexadiene; CaCO₃ / Pd(OH)2/C / ethanol

5: 87 percent / iPr₂NEt / CH₂Cl₂

6: 88 percent / Dess-Martin periodinane; pyridine / CH₂Cl₂

7: HF / acetonitrile / 0 °C

With pyridine; dmap; perchloric acid; 2,5-dihydrotoluene; hydrogen fluoride; Dess-Martin periodane; N-ethyl-N,N-diisopropylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; calcium carbonate; palladium dihydroxide; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile;
DOI:10.1002/1521-3773(20010105)40:1<191::AID-ANIE191>3.0.CO;2-C