C₁₈H₃₂O₃Si

Base Information

Chemical Name:C₁₈H₃₂O₃Si
CAS No.:1398308-08-1
Molecular Formula:C₁₈H₃₂O₃Si
Molecular Weight:324.536
Hs Code.:

C<sub>18</sub>H<sub>32</sub>O<sub>3</sub>Si

Synonyms:C₁₈H₃₂O₃Si

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Chemical Property of C₁₈H₃₂O₃Si

Chemical Property:

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Technology Process of C₁₈H₃₂O₃Si

There total 8 articles about C₁₈H₃₂O₃Si 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%

: 1379822-84-0
(-)-(S)-1-phenyl-3-(tert-butyldimethylsilyloxy)-hex-5-ene

: 1398308-08-1
C₁₈H₃₂O₃Si

Guidance literature:: With 4-methylmorpholine N-oxide; In water; tert-butyl alcohol; for 12h; Reflux;
DOI:10.1016/j.tetasy.2012.06.015

Reference yield:

: 104-53-0
3-phenyl-propionaldehyde

: 1398308-08-1
C₁₈H₃₂O₃Si

Guidance literature:: Multi-step reaction with 4 steps

1: ammonium chloride; zinc / tetrahydrofuran; water / 0 - 25 °C

2: macroporous acrylic resin-immobilized Candida antarctica lipase B / di-isopropyl ether / 70 h / 25 °C / Inert atmosphere; Enzymatic reaction

3: 1H-imidazole; dmap / dichloromethane / 18 h / 25 °C / Inert atmosphere

4: 4-methylmorpholine N-oxide / water; tert-butyl alcohol / 12 h / Reflux

With 1H-imidazole; dmap; ammonium chloride; 4-methylmorpholine N-oxide; zinc; In tetrahydrofuran; dichloromethane; di-isopropyl ether; water; tert-butyl alcohol; 1: |Barbier Coupling Reaction;
DOI:10.1016/j.tetasy.2012.06.015

Reference yield:

: 60340-28-5
1-phenylhex-5-en-3-ol

: 1398308-08-1
C₁₈H₃₂O₃Si

Guidance literature:: Multi-step reaction with 3 steps

1: macroporous acrylic resin-immobilized Candida antarctica lipase B / di-isopropyl ether / 70 h / 25 °C / Inert atmosphere; Enzymatic reaction

2: 1H-imidazole; dmap / dichloromethane / 18 h / 25 °C / Inert atmosphere

3: 4-methylmorpholine N-oxide / water; tert-butyl alcohol / 12 h / Reflux

With 1H-imidazole; dmap; 4-methylmorpholine N-oxide; In dichloromethane; di-isopropyl ether; water; tert-butyl alcohol;
DOI:10.1016/j.tetasy.2012.06.015