6-{[(4-methoxybenzyl)oxy]methyl}-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-one

Base Information

Chemical Name:6-{[(4-methoxybenzyl)oxy]methyl}-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-one
CAS No.:1318792-93-6
Molecular Formula:C₂₂H₂₂O₄
Molecular Weight:350.414
Hs Code.:

Synonyms:6-{[(4-methoxybenzyl)oxy]methyl}-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-one

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Chemical Property of 6-{[(4-methoxybenzyl)oxy]methyl}-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-one

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Technology Process of 6-{[(4-methoxybenzyl)oxy]methyl}-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-one

There total 7 articles about 6-{[(4-methoxybenzyl)oxy]methyl}-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-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: 51.0%

: 1318792-92-5
3-[2-(4-hydroxy-3-{[(4-methoxybenzyl)oxy]methyl}-1-butynyl)phenyl]propanoic acid

: 1318792-93-6
6-{[(4-methoxybenzyl)oxy]methyl}-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-one

Guidance literature:: With dmap; 2,4,6-trichlorobenzoyl chloride; triethylamine; In tetrahydrofuran; toluene; for 2.5h; Reflux;
DOI:10.1016/j.tetlet.2011.06.024

Reference yield:

: 141273-91-8
methyl 3-(2-iodophenyl)propanoate

: 1318792-93-6
6-{[(4-methoxybenzyl)oxy]methyl}-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / 4.5 h / 20 °C

2.1: water / methanol / 17 h / 20 °C

3.1: trifluorormethanesulfonic acid / diethyl ether / 0 - 20 °C

4.1: lithium hydroxide monohydrate / methanol / 21 h / 20 °C

4.2: pH 7

5.1: dmap; 2,4,6-trichlorobenzoyl chloride; triethylamine / tetrahydrofuran; toluene / 2.5 h / Reflux

With dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; lithium hydroxide monohydrate; trifluorormethanesulfonic acid; 2,4,6-trichlorobenzoyl chloride; water; triethylamine; In tetrahydrofuran; methanol; diethyl ether; toluene; 1.1: Sonogashira coupling / 5.1: Yamaguchi macrolactonization;
DOI:10.1016/j.tetlet.2011.06.024

Reference yield:

: 1318792-90-3
methyl 3-{2-[4-hydroxy-3-(hydroxymethyl)-1-butynyl]phenyl}propanoate

: 1318792-93-6
6-{[(4-methoxybenzyl)oxy]methyl}-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: trifluorormethanesulfonic acid / diethyl ether / 0 - 20 °C

2.1: lithium hydroxide monohydrate / methanol / 21 h / 20 °C

2.2: pH 7

3.1: dmap; 2,4,6-trichlorobenzoyl chloride; triethylamine / tetrahydrofuran; toluene / 2.5 h / Reflux

With dmap; lithium hydroxide monohydrate; trifluorormethanesulfonic acid; 2,4,6-trichlorobenzoyl chloride; triethylamine; In tetrahydrofuran; methanol; diethyl ether; toluene; 3.1: Yamaguchi macrolactonization;
DOI:10.1016/j.tetlet.2011.06.024