C₂₇H₃₂N₂O₃SSi

Base Information

Chemical Name:C₂₇H₃₂N₂O₃SSi
CAS No.:1374354-14-9
Molecular Formula:C₂₇H₃₂N₂O₃SSi
Molecular Weight:492.714
Hs Code.:

C<sub>27</sub>H<sub>32</sub>N<sub>2</sub>O<sub>3</sub>SSi

Synonyms:

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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 C₂₇H₃₂N₂O₃SSi

Chemical Property:

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Technology Process of C₂₇H₃₂N₂O₃SSi

There total 6 articles about C₂₇H₃₂N₂O₃SSi 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:

: 1374354-13-8
C₂₇H₃₄N₂O₄SSi

: 1374354-14-9
C₂₇H₃₂N₂O₃SSi

Guidance literature:: With Burgess Reagent; triethylamine; In acetonitrile; at 80 ℃;
DOI:10.1016/j.bmcl.2012.03.067

Reference yield:

: 230623-72-0
(4-bromo-thiophene-2-ylmethoxy)-tert-butyl-dimethylsilane

: 1374354-14-9
C₂₇H₃₂N₂O₃SSi

Guidance literature:: Multi-step reaction with 4 steps

1: 1,3-bis[(diphenylphosphino)propane]dichloronickel(II)

2: n-butyllithium / tetrahydrofuran

3: dicyclohexyl-carbodiimide

4: Burgess Reagent; triethylamine / acetonitrile / 80 °C

With n-butyllithium; Burgess Reagent; 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; acetonitrile;
DOI:10.1016/j.bmcl.2012.03.067

Reference yield:

: 18791-75-8
4-Bromothiophen-2-aldehyde

: 1374354-14-9
C₂₇H₃₂N₂O₃SSi

Guidance literature:: Multi-step reaction with 6 steps

1: sodium tetrahydroborate / methanol

2: 1H-imidazole

3: 1,3-bis[(diphenylphosphino)propane]dichloronickel(II)

4: n-butyllithium / tetrahydrofuran

5: dicyclohexyl-carbodiimide

6: Burgess Reagent; triethylamine / acetonitrile / 80 °C

With 1H-imidazole; sodium tetrahydroborate; n-butyllithium; Burgess Reagent; 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1016/j.bmcl.2012.03.067