Acetic acid (3E,5E,7E)-10-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trienyl ester

Base Information

Chemical Name:Acetic acid (3E,5E,7E)-10-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trienyl ester
CAS No.:287198-98-5
Molecular Formula:C₂₄H₃₆O₃Si
Molecular Weight:400.634
Hs Code.:

Synonyms:Acetic acid (3E,5E,7E)-10-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trienyl ester

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Chemical Property of Acetic acid (3E,5E,7E)-10-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trienyl ester

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Technology Process of Acetic acid (3E,5E,7E)-10-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trienyl ester

There total 8 articles about Acetic acid (3E,5E,7E)-10-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trienyl ester 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: 81.0%

: 108-24-7
acetic anhydride

: 287199-02-4
(3E,5E,7E)-10-[4-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trien-1-ol

: 287198-98-5
Acetic acid (3E,5E,7E)-10-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trienyl ester

Guidance literature:: With pyridine; dmap; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/S0040-4039(00)00532-3

Reference yield:

: 107148-48-1
(E)-tetrahydro-2-<(3-hexen-5-ynyl)oxy>-2H-pyran

: 287198-98-5
Acetic acid (3E,5E,7E)-10-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trienyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: Bu₃SnCu(CN)Li / tetrahydrofuran / -40 °C

1.2: (CH₃CN)2PdCl₂ / dimethylformamide / 0.5 h / 20 °C

2.1: 80 percent / pyridinium p-toluenesulfonate / ethanol / 7 h / 55 °C

3.1: 81 percent / pyridine; DMAP / CH₂Cl₂ / 2 h / 20 °C

With pyridine; dmap; Bu₃SnCu(CN)Li; pyridinium p-toluenesulfonate; In tetrahydrofuran; ethanol; dichloromethane; 1.1: Addition / 1.2: Substitution / 2.1: Hydrolysis / 3.1: Acetylation;
DOI:10.1016/S0040-4039(00)00532-3

Reference yield:

: 161249-56-5
3-[4-(tert-butyl-dimethyl-silanyloxy)phenyl]propionic acid methyl ester

: 287198-98-5
Acetic acid (3E,5E,7E)-10-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-deca-3,5,7-trienyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 100 percent / LiAlH₄ / tetrahydrofuran / 0.5 h / 0 °C

2.1: 71 percent / pyridinium dichromate; 3 Angstroem mol. sieves / CH₂Cl₂ / 1 h / 20 °C

3.1: chromium(II)chloride / dioxane; tetrahydrofuran / 24 h / 15 °C

4.1: Bu₃SnCu(CN)Li / tetrahydrofuran / -40 °C

4.2: (CH₃CN)2PdCl₂ / dimethylformamide / 0.5 h / 20 °C

5.1: 80 percent / pyridinium p-toluenesulfonate / ethanol / 7 h / 55 °C

6.1: 81 percent / pyridine; DMAP / CH₂Cl₂ / 2 h / 20 °C

With pyridine; chromium dichloride; dmap; lithium aluminium tetrahydride; dipyridinium dichromate; 3 A molecular sieve; Bu₃SnCu(CN)Li; pyridinium p-toluenesulfonate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; 1.1: Reduction / 2.1: Oxidation / 3.1: Condensation / 4.1: Addition / 4.2: Substitution / 5.1: Hydrolysis / 6.1: Acetylation;
DOI:10.1016/S0040-4039(00)00532-3