C₃₆H₅₀INO₃Si₂

Base Information

Chemical Name:C₃₆H₅₀INO₃Si₂
CAS No.:1240239-61-5
Molecular Formula:C₃₆H₅₀INO₃Si₂
Molecular Weight:727.873
Hs Code.:

C<sub>36</sub>H<sub>50</sub>INO<sub>3</sub>Si<sub>2</sub>

Synonyms:C₃₆H₅₀INO₃Si₂

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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 C₃₆H₅₀INO₃Si₂

Chemical Property:

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Technology Process of C₃₆H₅₀INO₃Si₂

There total 1 articles about C₃₆H₅₀INO₃Si₂ 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: 99.0%

: 1240239-66-0
C₃₅H₄₈INO₃Si₂

: 74-88-4
methyl iodide

: 1240239-61-5
C₃₆H₅₀INO₃Si₂

Guidance literature:: C₃₅H₄₈INO₃Si₂; With lithium hexamethyldisilazane; In tetrahydrofuran; hexane; at 0 ℃; Inert atmosphere;

methyl iodide; In tetrahydrofuran; hexane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ol1009703

Reference yield:

: 1240239-61-5
C₃₆H₅₀INO₃Si₂

: C₃₆H₄₉NO₃Si₂

Guidance literature:: With carbon monoxide; palladium diacetate; triethylamine; triphenylphosphine; In methanol; N,N-dimethyl acetamide; at 70 ℃; under 760.051 Torr;
DOI:10.1021/ol1009703

Reference yield:

: 67-56-1
methanol

: 201230-82-2
carbon monoxide

: 1240239-61-5
C₃₆H₅₀INO₃Si₂

: C₃₆H₄₉NO₃Si₂

: C₃₈H₅₃NO₅Si₂

: 1240239-64-8
C₃₈H₅₃NO₅Si₂

: (RS)-methyl 2-[(RS)-3-{2-[(tert-butyldimethylsilyl)oxy]ethyl}-1-methyl-2-oxoindolin-3-yl]-4-[(tert-butyldiphenylsilyl)oxy]butanoate

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; dmap; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; trifuran-2-yl-phosphane; In N,N-dimethyl acetamide; at 70 ℃; for 24h; under 5171.62 Torr; stereospecific reaction; Autoclave;
DOI:10.1021/ol1009703