4-Hydroxy-3-(phenylMethoxy)-benzoic Acid Methyl Ester

Base Information

• Chemical Name: 4-Hydroxy-3-(phenylMethoxy)-benzoic Acid Methyl Ester
• CAS No.: 1037072-57-3
• Molecular Formula: C15H14O4
• Molecular Weight: 258.274
• Mol file: 1037072-57-3.mol

Synonyms:4-Hydroxy-3-(benzyloxy)-benzoic Acid Methyl Ester;4-Hydroxy-3-(phenylMethoxy)-benzoic Acid Methyl Ester

Chemical Property of 4-Hydroxy-3-(phenylMethoxy)-benzoic Acid Methyl Ester

Chemical Property:

• Storage Temp.: -20°C Freezer
• Solubility.: Chloroform (Slightly), Methanol (Slightly, Heated)

Purity/Quality:

4-Hydroxy-3-(benzyloxy)-benzoicAcidMethylEster ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: ,4-Dihydroxybenzoic Acid (D451680) derivative with antioxidant properties. Used in the synthesis of cis- and trans-dibenzo-30-crown-10 derivatives. 4-Hydroxy-3-(phenylMethoxy)-benzoic Acid Methyl Ester can be used in the synthesis of cis- and trans-dibenzo-30-crown-10 derivatives.

Technology Process of 4-Hydroxy-3-(phenylMethoxy)-benzoic Acid Methyl Ester

There total 1 articles about 4-Hydroxy-3-(phenylMethoxy)-benzoic Acid Methyl Ester 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: 50.0%

3,4-dihydroxybenzoic acid methyl ester (2150-43-8) + benzyl bromide (100-39-0) → methyl 3-(benzyloxy)-4-hydroxybenzoate (1037072-57-3) + methyl 4-(benzyloxy)-3-hydroxybenzoate (87687-75-0)

Guidance literature:

With potassium carbonate; In acetonitrile; for 24h; Heating;

DOI:10.1021/jo800890x

Reference yield: 97.4%

methyl 3-(benzyloxy)-4-hydroxybenzoate (1037072-57-3) + 2-bromo-1-(6-methoxypyridin-3-yl)ethan-1-one → methyl 3-(benzyloxy)-4-[2-(6-methoxypyridin-3-yl)-2-oxoethoxy]benzoate

Guidance literature:

With caesium carbonate; In acetonitrile; at 30 ℃; for 2h;

Reference yield: 90.0%

methyl 3-(benzyloxy)-4-hydroxybenzoate (1037072-57-3) + C23H29ClO7 (1037072-52-8) → 1-(2-benzyloxy-5-carbomethoxy-phenoxy)-11-(2-benzyloxy-4-carbomethoxy-phenoxy)-3,6,9-trioxaundecane (1037072-54-0)

Guidance literature:

With potassium carbonate; In acetonitrile; for 36h; Heating;

DOI:10.1021/jo800890x

upstream raw materials:

3,4-dihydroxybenzoic acid methyl ester

benzyl bromide

Downstream raw materials:

1-(2-benzyloxy-5-carbomethoxy-phenoxy)-11-(2-benzyloxy-4-carbomethoxy-phenoxy)-3,6,9-trioxaundecane

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