N-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide

Base Information

Chemical Name:N-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide
CAS No.:791814-52-3
Molecular Formula:C₂₄H₂₇NO₅
Molecular Weight:409.482
Hs Code.:

<i>N</i>-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide

Synonyms:N-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide

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Chemical Property of N-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide

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Technology Process of N-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide

There total 7 articles about N-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide 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: 98.0%

: 72563-39-4
diethyl <(N-methylcarbamoyl)methyl>phosphonate

: 791814-40-9
6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxole-5-carbaldehyde

: 791814-52-3
N-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide

Guidance literature:: With sodium hydroxide; tetrahexylammonium iodide; In dichloromethane;
DOI:10.1021/jo049157q

Reference yield:

: 110-87-2
3,4-dihydro-2H-pyran

: 791814-52-3
N-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: 72 percent / camphorsulfonic acid monohydrate / CH₂Cl₂ / 20 °C

2.1: n-BuLi / tetrahydrofuran; hexane / 0.25 h / -78 °C

2.2: trimethyl borate / tetrahydrofuran; hexane / 1.25 h / cooling

3.1: 77 percent / Pd(OAc)2; Ph₃P; aq. NaHCO₃ / dioxane / 12 h / Heating

4.1: 98 percent / tetrahexylammonium iodide; aq. NaOH / CH₂Cl₂

With palladium diacetate; sodium hydroxide; n-butyllithium; camphor-10-sulfonic acid; sodium hydrogencarbonate; tetrahexylammonium iodide; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; hexane; dichloromethane; 3.1: Suzuki coupling;
DOI:10.1021/jo049157q

Reference yield:

: 120-57-0,30024-74-9
piperonal

: 791814-52-3
N-methyl-3-(6-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-benzo[1,3]dioxol-5-yl)-acrylamide

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / Br₂; FeCl₃; AcOH

2: 77 percent / Pd(OAc)2; Ph₃P; aq. NaHCO₃ / dioxane / 12 h / Heating

3: 98 percent / tetrahexylammonium iodide; aq. NaOH / CH₂Cl₂

With palladium diacetate; sodium hydroxide; bromine; iron(III) chloride; sodium hydrogencarbonate; tetrahexylammonium iodide; acetic acid; triphenylphosphine; In 1,4-dioxane; dichloromethane; 2: Suzuki coupling;
DOI:10.1021/jo049157q