2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetic acid

Base Information

• Chemical Name: 2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetic acid
• CAS No.: 1444311-43-6
• Molecular Formula: C₁₆H₁₈N₂O₄
• Molecular Weight: 302.33
• Mol file: 1444311-43-6.mol

Synonyms:2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetic acid

Chemical Property of 2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetic acid

There total 4 articles about 2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetic acid 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: 99.9%

ethyl 2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetate (1444311-27-6) → 2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetic acid (1444311-43-6)

Guidance literature:

With water; sodium hydroxide; at 60 - 80 ℃;

DOI:10.1016/j.ejmech.2013.03.066

Reference yield:

4-oxohexanoic acid (1117-74-4) → 2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetic acid (1444311-43-6)

Guidance literature:

Multi-step reaction with 4 steps

1: hydrazine hydrate / ethanol / 60 °C

2: potassium hydroxide / ethanol / Reflux

3: potassium carbonate / acetonitrile / Reflux

4: sodium hydroxide; water / 60 - 80 °C

With hydrazine hydrate; water; potassium carbonate; potassium hydroxide; sodium hydroxide; In ethanol; acetonitrile; 2: |Knoevenagel Condensation;

DOI:10.1016/j.ejmech.2013.03.066

Reference yield:

6-ethyl-4,5-dihydro-2H-pyridazin-3-one (412338-27-3) → 2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetic acid (1444311-43-6)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium hydroxide / ethanol / Reflux

2: potassium carbonate / acetonitrile / Reflux

3: sodium hydroxide; water / 60 - 80 °C

With water; potassium carbonate; potassium hydroxide; sodium hydroxide; In ethanol; acetonitrile; 1: |Knoevenagel Condensation;

DOI:10.1016/j.ejmech.2013.03.066

upstream raw materials:

4-oxohexanoic acid

6-ethyl-4,5-dihydro-2H-pyridazin-3-one

6-ethyl-4-(3-methoxybenzyl)pyridazin-3(2H)-one

ethyl 2-[3-ethyl-5-(3-methoxybenzyl)-6-oxopyridazin-1(6H)-yl]acetate