(Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-yl benzoate

Base Information

Chemical Name:(Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-yl benzoate
CAS No.:1398245-49-2
Molecular Formula:C₂₇H₃₈O₅Si
Molecular Weight:470.681
Hs Code.:

Synonyms:(Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-yl benzoate

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Chemical Property of (Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-yl benzoate

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Technology Process of (Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-yl benzoate

There total 9 articles about (Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-yl benzoate 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: 100.0%

: 1398247-72-7
(S,Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-ol

: 98-88-4
benzoyl chloride

: 1398245-49-2
(Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-yl benzoate

Guidance literature:: With pyridine; dmap; In dichloromethane; at 0 - 20 ℃; for 3h;
DOI:10.1021/jo3016055

Reference yield:

: 1398243-17-8
3-(2,5-dimethoxy-4-methylphenoxy)-3-methylbutane-1,2-diol

: 1398245-49-2
(Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-yl benzoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine; dmap / dichloromethane / 4 h / 20 °C / Inert atmosphere

2.1: potassium carbonate / methanol / 1 h / 20 °C / Inert atmosphere

3.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

3.2: 0.17 h / -78 °C / Inert atmosphere

3.3: 1 h / -78 °C / Inert atmosphere

4.1: quinoline; hydrogen / ethyl acetate / 1 h / 50 °C

5.1: dmap; pyridine / dichloromethane / 3 h / 0 - 20 °C

With pyridine; quinoline; dmap; n-butyllithium; hydrogen; potassium carbonate; triethylamine; In tetrahydrofuran; methanol; hexane; dichloromethane; ethyl acetate;
DOI:10.1021/jo3016055

Reference yield:

: 4925-88-6
2,5-dimethoxy-4-methylbenzaldehyde

: 1398245-49-2
(Z)-2-(2,5-dimethoxy-4-methylphenoxy)-2-methyl-7-(trimethylsilyl)hept-5-en-3-yl benzoate

Guidance literature:: Multi-step reaction with 8 steps

1.1: sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid / dichloromethane / 1 h / -10 °C / Inert atmosphere

1.2: 0.5 h / 20 °C / Inert atmosphere

2.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran / 3.5 h / 20 °C / Inert atmosphere

3.1: 4-methylmorpholine N-oxide; osmium(VIII) oxide / water; acetone / 3.5 h / 20 °C

4.1: triethylamine; dmap / dichloromethane / 4 h / 20 °C / Inert atmosphere

5.1: potassium carbonate / methanol / 1 h / 20 °C / Inert atmosphere

6.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

6.2: 0.17 h / -78 °C / Inert atmosphere

6.3: 1 h / -78 °C / Inert atmosphere

7.1: quinoline; hydrogen / ethyl acetate / 1 h / 50 °C

8.1: dmap; pyridine / dichloromethane / 3 h / 0 - 20 °C

With pyridine; quinoline; dmap; osmium(VIII) oxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; hydrogen; sodium hydrogencarbonate; potassium carbonate; 4-methylmorpholine N-oxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; methanol; hexane; dichloromethane; water; ethyl acetate; acetone;
DOI:10.1021/jo3016055