(E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-enyl)-5-isobutoxy-4H-chromen-4-one

Base Information

Chemical Name:(E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-enyl)-5-isobutoxy-4H-chromen-4-one
CAS No.:1422452-48-9
Molecular Formula:C₂₂H₂₀O₅
Molecular Weight:364.398
Hs Code.:

Synonyms:(E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-enyl)-5-isobutoxy-4H-chromen-4-one

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Chemical Property of (E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-enyl)-5-isobutoxy-4H-chromen-4-one

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Technology Process of (E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-enyl)-5-isobutoxy-4H-chromen-4-one

There total 7 articles about (E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-enyl)-5-isobutoxy-4H-chromen-4-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: 44.0%

: 1422452-74-1
(E)-5-isobutoxy-3-(3-(4-(4-methoxybenzyloxy)phenyl)-3-oxoprop-1-enyl)-4H-chromen-4-one

: 1422452-48-9
(E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-enyl)-5-isobutoxy-4H-chromen-4-one

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1016/j.ejmech.2012.11.007

Reference yield:

: 699-83-2
2,6-dihydroxylacetophenone

: 1422452-48-9
(E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-enyl)-5-isobutoxy-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate; sodium iodide / water; acetonitrile / Reflux

2: trichlorophosphate / 20 °C

3: dichloromethane / 20 °C

4: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

With potassium carbonate; trifluoroacetic acid; sodium iodide; trichlorophosphate; In dichloromethane; water; acetonitrile; 3: |Wittig Olefination / 4: |Wittig Olefination;
DOI:10.1016/j.ejmech.2012.11.007

Reference yield:

: 928634-22-4
1-(2-hydroxy-6-isobutoxyphenyl)ethanone

: 1422452-48-9
(E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-enyl)-5-isobutoxy-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: trichlorophosphate / 20 °C

2: dichloromethane / 20 °C

3: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

With trifluoroacetic acid; trichlorophosphate; In dichloromethane; 2: |Wittig Olefination / 3: |Wittig Olefination;
DOI:10.1016/j.ejmech.2012.11.007