1-bromomethyl-3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene

Base Information

• Chemical Name: 1-bromomethyl-3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene
• CAS No.: 870094-62-5
• Molecular Formula: C₂₈H₄₉BrO₇
• Molecular Weight: 577.597
• Mol file: 870094-62-5.mol

Synonyms:1-bromomethyl-3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene

Chemical Property of 1-bromomethyl-3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-bromomethyl-3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene

There total 3 articles about 1-bromomethyl-3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene 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: 88.0%

{3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-phenyl}-methanol (870094-61-4) → 1-bromomethyl-3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene (870094-62-5)

Guidance literature:

With N-Bromosuccinimide; triphenylphosphine; In tetrahydrofuran; at 20 ℃;

DOI:10.1021/ja054542y

Reference yield:

3,6,9,12,15-pentaoxahexadecyl tosylate (80755-67-5,58320-73-3) → 1-bromomethyl-3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene (870094-62-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 96 percent / potassium carbonate; 18-crown-6 / acetone / Heating

2: 88 percent / triphenylphosphine; N-bromosuccinimide / tetrahydrofuran / 20 °C

With N-Bromosuccinimide; 18-crown-6 ether; potassium carbonate; triphenylphosphine; In tetrahydrofuran; acetone;

DOI:10.1021/ja054542y

Reference yield:

3-decyloxy-5-hydroxybenzyl alcohol (474960-31-1) → 1-bromomethyl-3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene (870094-62-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 96 percent / potassium carbonate; 18-crown-6 / acetone / Heating

2: 88 percent / triphenylphosphine; N-bromosuccinimide / tetrahydrofuran / 20 °C

With N-Bromosuccinimide; 18-crown-6 ether; potassium carbonate; triphenylphosphine; In tetrahydrofuran; acetone;

DOI:10.1021/ja054542y

upstream raw materials:

{3-decyloxy-5-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-phenyl}-methanol

3,6,9,12,15-pentaoxahexadecyl tosylate

3-decyloxy-5-hydroxybenzyl alcohol

Downstream raw materials:

C₈₂H₁₃₀O₁₉

C₈₃H₁₃₂O₂₄

C₈₂H₁₃₀O₁₉