1-(7-bromo-6-hydroxy-4-methoxy-1-benzofuran-5-yl)-3-(4-chlorophenyl)prop-2-en-1-one

Base Information

Chemical Name:1-(7-bromo-6-hydroxy-4-methoxy-1-benzofuran-5-yl)-3-(4-chlorophenyl)prop-2-en-1-one
CAS No.:1350717-55-3
Molecular Formula:C₁₈H₁₂BrClO₄
Molecular Weight:407.648
Hs Code.:

Synonyms:1-(7-bromo-6-hydroxy-4-methoxy-1-benzofuran-5-yl)-3-(4-chlorophenyl)prop-2-en-1-one

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Chemical Property of 1-(7-bromo-6-hydroxy-4-methoxy-1-benzofuran-5-yl)-3-(4-chlorophenyl)prop-2-en-1-one

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Technology Process of 1-(7-bromo-6-hydroxy-4-methoxy-1-benzofuran-5-yl)-3-(4-chlorophenyl)prop-2-en-1-one

There total 3 articles about 1-(7-bromo-6-hydroxy-4-methoxy-1-benzofuran-5-yl)-3-(4-chlorophenyl)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: 83.0%

: 73877-35-7
1-(7-bromo-6-hydroxy-4-methoxy benzofuran-5-yl)ethanone

: 104-88-1
4-chlorobenzaldehyde

: 1350717-55-3
1-(7-bromo-6-hydroxy-4-methoxy-1-benzofuran-5-yl)-3-(4-chlorophenyl)prop-2-en-1-one

Guidance literature:: With sodium hydroxide; In ethanol; at 20 ℃; for 24h;
DOI:10.1016/j.ejmech.2014.06.007

Reference yield:

: 82-57-5
visnagin

: 1350717-55-3
1-(7-bromo-6-hydroxy-4-methoxy-1-benzofuran-5-yl)-3-(4-chlorophenyl)prop-2-en-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: bromine; acetic acid

2: water; potassium hydroxide

3: sodium hydroxide / ethanol; water / 20 °C

With water; bromine; acetic acid; potassium hydroxide; sodium hydroxide; In ethanol; water;
DOI:10.1007/s12272-011-1006-2

Reference yield:

: 96583-74-3
9-bromo-4-methoxy-7-methyl-5H-furo[3,2-g]chromen-5-one

: 1350717-55-3
1-(7-bromo-6-hydroxy-4-methoxy-1-benzofuran-5-yl)-3-(4-chlorophenyl)prop-2-en-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / 1 h / Reflux

2: sodium hydroxide / ethanol / 24 h / 20 °C

With potassium hydroxide; sodium hydroxide; In ethanol; 2: |Claisen-Schmidt Condensation;
DOI:10.1016/j.ejmech.2014.06.007