<2-<3-(2-Methyl-1,3-dioxolan-2-yl)propyl>-1,3-dithian-2-yl>methyldiphenylsilane

Base Information

Chemical Name:<2-<3-(2-Methyl-1,3-dioxolan-2-yl)propyl>-1,3-dithian-2-yl>methyldiphenylsilane
CAS No.:1026491-28-0
Molecular Formula:C₂₄H₃₂O₂S₂Si
Molecular Weight:444.734
Hs Code.:

Synonyms:<2-<3-(2-Methyl-1,3-dioxolan-2-yl)propyl>-1,3-dithian-2-yl>methyldiphenylsilane

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of <2-<3-(2-Methyl-1,3-dioxolan-2-yl)propyl>-1,3-dithian-2-yl>methyldiphenylsilane

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Technology Process of <2-<3-(2-Methyl-1,3-dioxolan-2-yl)propyl>-1,3-dithian-2-yl>methyldiphenylsilane

There total 2 articles about <2-<3-(2-Methyl-1,3-dioxolan-2-yl)propyl>-1,3-dithian-2-yl>methyldiphenylsilane 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: 94.0%

: 5978-08-5
1-chloro-4-(1,3-dioxolane)-n-pentane

: 135746-47-3
2-methyldiphenylsilyl-1,3-dithiane

: 1026491-28-0
<2-<3-(2-Methyl-1,3-dioxolan-2-yl)propyl>-1,3-dithian-2-yl>methyldiphenylsilane

Guidance literature:: With n-butyllithium; 1.) THF, hexane, -25 deg C, 2.5 h, 2.) HMPA, -25 deg C, 1 h;
DOI:10.1021/jo00106a025

Reference yield:

: 144-79-6
chloromethyldiphenylsilane

: 1026491-28-0
<2-<3-(2-Methyl-1,3-dioxolan-2-yl)propyl>-1,3-dithian-2-yl>methyldiphenylsilane

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / n-BuLi / tetrahydrofuran; hexane / 1.) -25 deg C, 2.5 h, 2.) -40 deg C to r.t., overnight

2: 94 percent / n-BuLi / 1.) THF, hexane, -25 deg C, 2.5 h, 2.) HMPA, -25 deg C, 1 h

With n-butyllithium; In tetrahydrofuran; hexane;
DOI:10.1021/jo00106a025