(E)-3-(4-(benzyloxy)-2,3,6-trimethoxyphenyl)-1-(4-(benzyloxy)-3-methoxyphenyl)-prop-2-en-1-one

Base Information

Chemical Name:(E)-3-(4-(benzyloxy)-2,3,6-trimethoxyphenyl)-1-(4-(benzyloxy)-3-methoxyphenyl)-prop-2-en-1-one
CAS No.:1357024-86-2
Molecular Formula:C₃₃H₃₂O₇
Molecular Weight:540.613
Hs Code.:

Synonyms:(E)-3-(4-(benzyloxy)-2,3,6-trimethoxyphenyl)-1-(4-(benzyloxy)-3-methoxyphenyl)-prop-2-en-1-one

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Chemical Property of (E)-3-(4-(benzyloxy)-2,3,6-trimethoxyphenyl)-1-(4-(benzyloxy)-3-methoxyphenyl)-prop-2-en-1-one

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Technology Process of (E)-3-(4-(benzyloxy)-2,3,6-trimethoxyphenyl)-1-(4-(benzyloxy)-3-methoxyphenyl)-prop-2-en-1-one

There total 15 articles about (E)-3-(4-(benzyloxy)-2,3,6-trimethoxyphenyl)-1-(4-(benzyloxy)-3-methoxyphenyl)-prop-2-en-1-one 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: 69.0%

: 1835-11-6
4-benzyloxy-3-methoxyacetophenone

: 52249-82-8
4-(benzyloxy)-2,3,6-trimethoxybenzaldehyde

: 1357024-86-2
(E)-3-(4-(benzyloxy)-2,3,6-trimethoxyphenyl)-1-(4-(benzyloxy)-3-methoxyphenyl)-prop-2-en-1-one

Guidance literature:: With potassium hydroxide; In methanol; water; at 0 - 20 ℃; for 24.5h;
DOI:10.1016/j.ejmech.2011.12.008

Reference yield:

: 708-76-9
2-hydroxy-4,6-dimethoxybenzaldehyde

: 1357024-86-2
(E)-3-(4-(benzyloxy)-2,3,6-trimethoxyphenyl)-1-(4-(benzyloxy)-3-methoxyphenyl)-prop-2-en-1-one

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / N,N-dimethyl-formamide / 8 h / 80 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 4 h / 20 °C

3: sodium hydroxide / methanol / 3 h / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 6 h / 80 °C

5: trichlorophosphate / 3.5 h / 0 - 80 °C

6: potassium hydroxide / methanol; water / 24.5 h / 0 - 20 °C

With potassium carbonate; 3-chloro-benzenecarboperoxoic acid; potassium hydroxide; sodium hydroxide; trichlorophosphate; In methanol; dichloromethane; water; N,N-dimethyl-formamide; 2: Baeyer-Villiger oxidation / 5: Vilsmeier formylation / 6: Aldol condensation;
DOI:10.1016/j.ejmech.2011.12.008

Reference yield:

: 3-benzyloxy-4,5-dimethoxyphenol

: 1357024-86-2
(E)-3-(4-(benzyloxy)-2,3,6-trimethoxyphenyl)-1-(4-(benzyloxy)-3-methoxyphenyl)-prop-2-en-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetone

2: trichlorophosphate / 3.5 h / 0 - 80 °C

3: potassium hydroxide / methanol; water / 24.5 h / 0 - 20 °C

With potassium carbonate; potassium hydroxide; trichlorophosphate; In methanol; water; acetone; 2: Vilsmeier formylation / 3: Aldol condensation;
DOI:10.1016/j.ejmech.2011.12.008