C₃₅H₆₂O₆Si

Base Information

Chemical Name:C₃₅H₆₂O₆Si
CAS No.:1003890-47-8
Molecular Formula:C₃₅H₆₂O₆Si
Molecular Weight:606.959
Hs Code.:

C<sub>35</sub>H<sub>62</sub>O<sub>6</sub>Si

Synonyms:C₃₅H₆₂O₆Si

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Chemical Property of C₃₅H₆₂O₆Si

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Technology Process of C₃₅H₆₂O₆Si

There total 9 articles about C₃₅H₆₂O₆Si 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: 96.0%

: 1003890-60-5
C₃₀H₅₂O₆Si

: 53750-52-0
4-iodo-2-methyl-but-1-ene

: 1003890-47-8
C₃₅H₆₂O₆Si

Guidance literature:: 4-iodo-2-methyl-but-1-ene; With magnesium; In diethyl ether; Heating;

C₃₀H₅₂O₆Si; In diethyl ether; at -78 - 20 ℃; Further stages.;
DOI:10.1021/ol7025944

Reference yield:

: 887143-81-9
(1S,6R,8R)-8-Vinyl-2,9,10-trioxa-1-phospha-bicyclo[4.3.1]dec-4-ene 1-oxide

: 1003890-47-8
C₃₅H₆₂O₆Si

Guidance literature:: Multi-step reaction with 7 steps

1.1: Hoveyda-Grubbs catalyst second generation / 1,1-dichloroethane / 90 °C / Inert atmosphere

2.1: 2-nitrobenzenesulfonyl hydrazide; triethylamine / 1,2-dichloro-ethane / Inert atmosphere

3.1: formic acid; palladium diacetate; triethylamine / 1,2-dichloro-ethane / 40 °C / Inert atmosphere

3.2: Inert atmosphere

4.1: lithium aluminium tetrahydride / diethyl ether / Inert atmosphere

5.1: pyridinium p-toluenesulfonate / dichloromethane / Inert atmosphere

6.1: pyridine; ozone / methanol; dichloromethane / -78 °C / Inert atmosphere

6.2: Inert atmosphere

7.1: magnesium / diethyl ether / -78 °C / Inert atmosphere

With pyridine; lithium aluminium tetrahydride; formic acid; Hoveyda-Grubbs catalyst second generation; 2-nitrobenzenesulfonyl hydrazide; palladium diacetate; pyridinium p-toluenesulfonate; ozone; magnesium; triethylamine; In methanol; diethyl ether; 1,1-dichloroethane; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1021/jo2003506

Reference yield:

: 887343-98-8
(4R,6R)-2-Allyloxy-4,6-divinyl-[1,3,2]dioxaphosphinane 2-oxide

: 1003890-47-8
C₃₅H₆₂O₆Si

Guidance literature:: Multi-step reaction with 8 steps

1.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane

2.1: Hoveyda-Grubbs catalyst second generation / 1,1-dichloroethane / 90 °C / Inert atmosphere

3.1: 2-nitrobenzenesulfonyl hydrazide; triethylamine / 1,2-dichloro-ethane / Inert atmosphere

4.1: formic acid; palladium diacetate; triethylamine / 1,2-dichloro-ethane / 40 °C / Inert atmosphere

4.2: Inert atmosphere

5.1: lithium aluminium tetrahydride / diethyl ether / Inert atmosphere

6.1: pyridinium p-toluenesulfonate / dichloromethane / Inert atmosphere

7.1: pyridine; ozone / methanol; dichloromethane / -78 °C / Inert atmosphere

7.2: Inert atmosphere

8.1: magnesium / diethyl ether / -78 °C / Inert atmosphere

With pyridine; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; lithium aluminium tetrahydride; formic acid; Hoveyda-Grubbs catalyst second generation; 2-nitrobenzenesulfonyl hydrazide; palladium diacetate; pyridinium p-toluenesulfonate; ozone; magnesium; triethylamine; In methanol; diethyl ether; 1,1-dichloroethane; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1021/jo2003506