(E)-1-(4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-3-(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)prop-2-en-1-one

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Chemical Name:(E)-1-(4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-3-(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)prop-2-en-1-one
CAS No.:1385690-97-0
Molecular Formula:C₃₅H₂₉N₃O₅
Molecular Weight:571.632
Hs Code.:

Synonyms:(E)-1-(4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-3-(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)prop-2-en-1-one

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Chemical Property of (E)-1-(4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-3-(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)prop-2-en-1-one

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Technology Process of (E)-1-(4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-3-(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)prop-2-en-1-one

There total 3 articles about (E)-1-(4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-3-(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)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: 85.0%

: 21487-49-0
3-(4-nitrophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde

: 1385690-74-3
1-[4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl]ethanone

: 1385690-97-0
(E)-1-(4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-3-(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)prop-2-en-1-one

Guidance literature:: With sodium hydroxide; In ethanol; at 20 ℃;
DOI:10.1016/j.bmcl.2012.05.016

Reference yield:

: 118683-88-8
1-[2-hydroxy-4-(2-methyl-allyloxy)-phenyl]-ethanone

: 1385690-97-0
(E)-1-(4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-3-(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)prop-2-en-1-one

Guidance literature:: Multi-step reaction with 4 steps

1: N,N-diethylaniline / 4 h / 220 °C

2: toluene-4-sulfonic acid / chloroform / 6 h / 20 °C

3: potassium carbonate / acetone / 6 h / Reflux

4: sodium hydroxide / ethanol / 20 °C

With potassium carbonate; toluene-4-sulfonic acid; N,N-diethylaniline; sodium hydroxide; In ethanol; chloroform; acetone; 1: Claisen rearrangement;
DOI:10.1016/j.bmcl.2012.05.016

Reference yield:

: 1385690-73-2
1-(4-hydroxy-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)ethanone

: 1385690-97-0
(E)-1-(4-(benzyloxy)-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-3-(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)prop-2-en-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetone / 6 h / Reflux

2: sodium hydroxide / ethanol / 20 °C

With potassium carbonate; sodium hydroxide; In ethanol; acetone;
DOI:10.1016/j.bmcl.2012.05.016