N-(((1-(4-methoxyphenyl)vinyl)oxy)dimethylsilyl)-4-methyl-N-(trimethylsilyl)benzenesulfonamide

Base Information

Chemical Name:N-(((1-(4-methoxyphenyl)vinyl)oxy)dimethylsilyl)-4-methyl-N-(trimethylsilyl)benzenesulfonamide
CAS No.:1638623-46-7
Molecular Formula:C₂₁H₃₁NO₄SSi₂
Molecular Weight:449.718
Hs Code.:

Synonyms:N-(((1-(4-methoxyphenyl)vinyl)oxy)dimethylsilyl)-4-methyl-N-(trimethylsilyl)benzenesulfonamide

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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 N-(((1-(4-methoxyphenyl)vinyl)oxy)dimethylsilyl)-4-methyl-N-(trimethylsilyl)benzenesulfonamide

Chemical Property:

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Technology Process of N-(((1-(4-methoxyphenyl)vinyl)oxy)dimethylsilyl)-4-methyl-N-(trimethylsilyl)benzenesulfonamide

There total 4 articles about N-(((1-(4-methoxyphenyl)vinyl)oxy)dimethylsilyl)-4-methyl-N-(trimethylsilyl)benzenesulfonamide 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:

: C₁₁H₁₅ClO₂Si

: 1015-42-5
p-toluenesulfonyl-N-trimethylsilylamine

: 1638623-46-7
N-(((1-(4-methoxyphenyl)vinyl)oxy)dimethylsilyl)-4-methyl-N-(trimethylsilyl)benzenesulfonamide

Guidance literature:: With triethylamine; In acetonitrile; pentane; at 0 ℃; Inert atmosphere; Schlenk technique;
DOI:10.1002/anie.201400405

Reference yield:

: 70-55-3
toluene-4-sulfonamide

: 1638623-46-7
N-(((1-(4-methoxyphenyl)vinyl)oxy)dimethylsilyl)-4-methyl-N-(trimethylsilyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: n-butyllithium / dichloromethane; hexane / 4 h / 0 °C / Inert atmosphere; Schlenk technique

2: triethylamine / acetonitrile; pentane / 0 °C / Inert atmosphere; Schlenk technique

With n-butyllithium; triethylamine; In hexane; dichloromethane; acetonitrile; pentane;
DOI:10.1002/anie.201400405

Reference yield:

: N,N-diethyl-1-((1-(4-methoxyphenyl)vinyl)oxy)-1,1-dimethylsilanamine

: 1638623-46-7
N-(((1-(4-methoxyphenyl)vinyl)oxy)dimethylsilyl)-4-methyl-N-(trimethylsilyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: acetyl chloride / tetrahydrofuran / 0.33 h / 0 °C / Inert atmosphere; Schlenk technique

2: triethylamine / acetonitrile; pentane / 0 °C / Inert atmosphere; Schlenk technique

With triethylamine; acetyl chloride; In tetrahydrofuran; acetonitrile; pentane;
DOI:10.1002/anie.201400405