(6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-2-(5-methylfuran-2-yl)-benzofuran-3-yl)(3,4,5-trimethoxyphenyl)methanone

Base Information

Chemical Name:(6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-2-(5-methylfuran-2-yl)-benzofuran-3-yl)(3,4,5-trimethoxyphenyl)methanone
CAS No.:1359976-94-5
Molecular Formula:C₃₅H₃₁NO₈
Molecular Weight:593.633
Hs Code.:

Synonyms:(6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-2-(5-methylfuran-2-yl)-benzofuran-3-yl)(3,4,5-trimethoxyphenyl)methanone

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Chemical Property of (6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-2-(5-methylfuran-2-yl)-benzofuran-3-yl)(3,4,5-trimethoxyphenyl)methanone

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Technology Process of (6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-2-(5-methylfuran-2-yl)-benzofuran-3-yl)(3,4,5-trimethoxyphenyl)methanone

There total 8 articles about (6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-2-(5-methylfuran-2-yl)-benzofuran-3-yl)(3,4,5-trimethoxyphenyl)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: 34.9%

: 1359977-05-1
5-methyl-4-(2-(2-(5-methylfuran-2-yl)benzofuran-6-yloxy)ethyl)-2-phenyl-oxazole

: 4521-61-3
3,4,5-Trimethoxybenzoyl chloride

: 1359976-94-5
(6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-2-(5-methylfuran-2-yl)-benzofuran-3-yl)(3,4,5-trimethoxyphenyl)methanone

Guidance literature:: With tin(IV) chloride; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1016/j.ejmech.2012.05.013

Reference yield:

: 52085-14-0
4-benzoxy-salicylaldehyde

: 1359976-94-5
(6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-2-(5-methylfuran-2-yl)-benzofuran-3-yl)(3,4,5-trimethoxyphenyl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1: titanium tetrachloride; zinc / tetrahydrofuran / Inert atmosphere; Reflux

2: iodine; potassium carbonate / tetrahydrofuran / 20 °C

3: titanium tetrachloride / dichloromethane / 20 °C

4: potassium carbonate / acetonitrile / Reflux

5: tin(IV) chloride / dichloromethane / 12 h / 20 °C

With iodine; titanium tetrachloride; tin(IV) chloride; potassium carbonate; zinc; In tetrahydrofuran; dichloromethane; acetonitrile; 5: Friedel Crafts acylation;
DOI:10.1016/j.ejmech.2012.05.013

Reference yield:

: 103788-65-4
(5-methyl-2-phenyloxazol-4-yl)ethanol

: 1359976-94-5
(6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-2-(5-methylfuran-2-yl)-benzofuran-3-yl)(3,4,5-trimethoxyphenyl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 1 h / 0 - 20 °C

2: potassium carbonate / acetonitrile / Reflux

3: tin(IV) chloride / dichloromethane / 12 h / 20 °C

With tin(IV) chloride; potassium carbonate; triethylamine; In dichloromethane; acetonitrile; 3: Friedel Crafts acylation;
DOI:10.1016/j.ejmech.2012.05.013