6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde

Base Information

Chemical Name:6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde
CAS No.:258283-82-8
Molecular Formula:C₁₈H₁₇BrO₆
Molecular Weight:409.233
Hs Code.:

Synonyms:6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde

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Chemical Property of 6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde

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Technology Process of 6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde

There total 9 articles about 6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde 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: 60.0%

: 18173-64-3
tert-butyldimethylsilanol

: C₁₉H₂₀O₇

: 258283-82-8
6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde

Guidance literature:: In dichloromethane; at 25 ℃; for 15h;
DOI:10.1002/ejoc.201402761

Reference yield:

: methanesulfonic acid 2-(6-formyl-benzo[1,3]dioxol-5-yl)-3,4,5-trimethoxy-benzyl ester

: 258283-82-8
6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde

Guidance literature:: With lithium bromide; In acetone;
DOI:10.1021/ja9930059

Reference yield:

: 64490-45-5
2-iodo-3,4,5-trimethoxybenzyl alcohol

: 258283-82-8
6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1: 62 percent / Pd(PPh₃)4; aq. NaHCO₃ / 1,2-dimethoxy-ethane

2: Et₃N / CH₂Cl₂

3: LiBr / acetone

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydrogencarbonate; triethylamine; lithium bromide; In 1,2-dimethoxyethane; dichloromethane; acetone; 1: Suzuki coupling / 2: mesylation / 3: Substitution;
DOI:10.1021/ja9930059