[3-(1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-methoxy-6-(methoxymethoxy)phenyl](phenyl)methanone

Base Information

Chemical Name:[3-(1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-methoxy-6-(methoxymethoxy)phenyl](phenyl)methanone
CAS No.:1424077-28-0
Molecular Formula:C₂₄H₃₄O₅Si
Molecular Weight:430.616
Hs Code.:

Synonyms:[3-(1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-methoxy-6-(methoxymethoxy)phenyl](phenyl)methanone

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Chemical Property of [3-(1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-methoxy-6-(methoxymethoxy)phenyl](phenyl)methanone

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Technology Process of [3-(1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-methoxy-6-(methoxymethoxy)phenyl](phenyl)methanone

There total 5 articles about [3-(1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-methoxy-6-(methoxymethoxy)phenyl](phenyl)methanone 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: 78.0%

: 1424077-24-6
tert-butyl{1-[2-methoxy-4-(methoxymethoxy)phenyl]ethoxy}dimethylsilane

: 98-88-4
benzoyl chloride

: 1424077-28-0
[3-(1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-methoxy-6-(methoxymethoxy)phenyl](phenyl)methanone

Guidance literature:: tert-butyl{1-[2-methoxy-4-(methoxymethoxy)phenyl]ethoxy}dimethylsilane; With n-butyllithium; In tetrahydrofuran; at 0 ℃; for 0.166667h;

benzoyl chloride; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1002/jccs.201200233

Reference yield:

: 89-84-9
2',4'-dihydroxy-4-acetophenone

: 1424077-28-0
[3-(1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-methoxy-6-(methoxymethoxy)phenyl](phenyl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C

2.1: potassium carbonate / acetone / 12 h / Reflux

3.1: sodium tetrahydroborate / methanol / 0 - 20 °C

4.1: triethylamine; 1H-imidazole / N,N-dimethyl-formamide / 24 h / 60 °C

5.1: n-butyllithium / tetrahydrofuran / 0.17 h / 0 °C

5.2: 0 - 20 °C

With 1H-imidazole; sodium tetrahydroborate; n-butyllithium; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1002/jccs.201200233

Reference yield:

: 65490-08-6
2-hydroxy-4-(methoxymethoxy)acetophenone

: 1424077-28-0
[3-(1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-2-methoxy-6-(methoxymethoxy)phenyl](phenyl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetone / 12 h / Reflux

2.1: sodium tetrahydroborate / methanol / 0 - 20 °C

3.1: triethylamine; 1H-imidazole / N,N-dimethyl-formamide / 24 h / 60 °C

4.1: n-butyllithium / tetrahydrofuran / 0.17 h / 0 °C

4.2: 0 - 20 °C

With 1H-imidazole; sodium tetrahydroborate; n-butyllithium; potassium carbonate; triethylamine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetone;
DOI:10.1002/jccs.201200233