tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane

Base Information

Chemical Name:tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane
CAS No.:303158-52-3
Molecular Formula:C₂₈H₄₀O₅Si
Molecular Weight:484.708
Hs Code.:

Synonyms:tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane

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Chemical Property of tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane

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Technology Process of tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane

There total 8 articles about tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane 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: 94.0%

: 107-30-2
chloromethyl methyl ether

: 303158-65-8
(E)-(R)-4-(tert-Butyl-diphenyl-silanyloxy)-4-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-methyl-but-2-en-1-ol

: 303158-52-3
tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/ol0063656

Reference yield:

: 18524-18-0
(R)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)prop-2-en-1-ol

: 303158-52-3
tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane

Guidance literature:: Multi-step reaction with 5 steps

1.1: 98 percent / imidazole / dimethylformamide

2.1: CH₂Cl₂

2.2: 98 percent / Me₂S

3.1: 96 percent / toluene / Heating

4.1: 95 percent / DIBAL / CH₂Cl₂ / 0 °C

5.1: 94 percent / i-Pr₂NEt / CH₂Cl₂

With 1H-imidazole; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; toluene; 1.1: silylation / 2.1: ozonation / 2.2: Reduction / 3.1: Wittig olefination / 4.1: Reduction / 5.1: Alkylation;
DOI:10.1021/ol0063656

Reference yield:

: 102357-25-5
(1S,4'R)-1-(2,2-dimethyl-1,3-dioxolane-4-yl)-2-trimethylsilylprop-2-en-1-ol

: 303158-52-3
tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane

Guidance literature:: Multi-step reaction with 6 steps

1.1: 95 percent / NaH; HMPA

2.1: 98 percent / imidazole / dimethylformamide

3.1: CH₂Cl₂

3.2: 98 percent / Me₂S

4.1: 96 percent / toluene / Heating

5.1: 95 percent / DIBAL / CH₂Cl₂ / 0 °C

6.1: 94 percent / i-Pr₂NEt / CH₂Cl₂

With 1H-imidazole; N,N,N,N,N,N-hexamethylphosphoric triamide; sodium hydride; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; toluene; 1.1: protodesilylation / 2.1: silylation / 3.1: ozonation / 3.2: Reduction / 4.1: Wittig olefination / 5.1: Reduction / 6.1: Alkylation;
DOI:10.1021/ol0063656