1,3-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(E)-8-(1-ethoxy-ethoxy)-oct-1-enyl]-benzene

Base Information

Chemical Name:1,3-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(E)-8-(1-ethoxy-ethoxy)-oct-1-enyl]-benzene
CAS No.:205523-89-3
Molecular Formula:C₃₀H₅₆O₄Si₂
Molecular Weight:536.943
Hs Code.:

Synonyms:1,3-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(E)-8-(1-ethoxy-ethoxy)-oct-1-enyl]-benzene

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Chemical Property of 1,3-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(E)-8-(1-ethoxy-ethoxy)-oct-1-enyl]-benzene

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Technology Process of 1,3-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(E)-8-(1-ethoxy-ethoxy)-oct-1-enyl]-benzene

There total 8 articles about 1,3-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(E)-8-(1-ethoxy-ethoxy)-oct-1-enyl]-benzene 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:

: 10160-24-4
7-bromoheptyl alcohol

: 205523-89-3
1,3-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(E)-8-(1-ethoxy-ethoxy)-oct-1-enyl]-benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / TsOH / CH₂Cl₂ / 0.17 h / 0 °C

2: 50 percent / DMSO, NaHCO₃ / 3 h / 120 °C

3: 1.) BuLi / 1.) THF, r.t., 75 min, 2.) THF, r.t., overnight

With n-butyllithium; sodium hydrogencarbonate; toluene-4-sulfonic acid; dimethyl sulfoxide; In dichloromethane;
DOI:10.1055/s-1998-2193

Reference yield:

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 205523-89-3
1,3-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(E)-8-(1-ethoxy-ethoxy)-oct-1-enyl]-benzene

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / Et₃N / tetrahydrofuran / Ambient temperature

2: 100 percent / LiAlH₄ / diethyl ether / 2 h / Ambient temperature

3: 87 percent / PPh₃, CCl₄ / 2 h / 110 °C

4: 86 percent / 5 h / 100 °C

5: 1.) BuLi / 1.) THF, r.t., 75 min, 2.) THF, r.t., overnight

With tetrachloromethane; lithium aluminium tetrahydride; n-butyllithium; triethylamine; triphenylphosphine; In tetrahydrofuran; diethyl ether;
DOI:10.1055/s-1998-2193

Reference yield:

: 103929-83-5
methyl 3,5-bis(tert-butyldimethylsilyloxy)benzoate

: 205523-89-3
1,3-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(E)-8-(1-ethoxy-ethoxy)-oct-1-enyl]-benzene

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / LiAlH₄ / diethyl ether / 2 h / Ambient temperature

2: 87 percent / PPh₃, CCl₄ / 2 h / 110 °C

3: 86 percent / 5 h / 100 °C

4: 1.) BuLi / 1.) THF, r.t., 75 min, 2.) THF, r.t., overnight

With tetrachloromethane; lithium aluminium tetrahydride; n-butyllithium; triphenylphosphine; In diethyl ether;
DOI:10.1055/s-1998-2193