2-((3-Methoxybenzyl)oxy)isoindoline-1,3-dione

Base Information

• Chemical Name: 2-((3-Methoxybenzyl)oxy)isoindoline-1,3-dione
• CAS No.: 2014-60-0
• Molecular Formula: C16H13NO4
• Molecular Weight: 283.284
• DSSTox Substance ID: DTXSID001204138

Synonyms:2014-60-0;2-((3-methoxybenzyl)oxy)isoindoline-1,3-dione;2-[(3-methoxyphenyl)methoxy]isoindole-1,3-dione;1H-Isoindole-1,3(2H)-dione, 2-[(3-methoxyphenyl)methoxy]-;2-[(3-methoxyphenyl)methoxy]-2,3-dihydro-1H-isoindole-1,3-dione;Oprea1_407689;SCHEMBL5524437;DTXSID001204138;AKOS005091642;4F-917;2-[(3-Methoxyphenyl)methoxy]-1H-isoindole-1,3(2H)-dione

Chemical Property of 2-((3-Methoxybenzyl)oxy)isoindoline-1,3-dione

Chemical Property:

• XLogP3: 2.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 283.08445790
• Heavy Atom Count: 21
• Complexity: 387

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC1=CC=CC(=C1)CON2C(=O)C3=CC=CC=C3C2=O

Technology Process of 2-((3-Methoxybenzyl)oxy)isoindoline-1,3-dione

There total 4 articles about 2-((3-Methoxybenzyl)oxy)isoindoline-1,3-dione 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: 94.0%

N-hydroxyphthalimide (524-38-9) + 1-bromomethyl-3-methoxybenzene (874-98-6) → 2-[(3-methoxyphenyl)methoxy]-1H-isoindole-1,3(2H)-dione (2014-60-0)

Guidance literature:

N-hydroxyphthalimide; With sodium hydride; In N,N-dimethyl-formamide;

1-bromomethyl-3-methoxybenzene; With sodium iodide; In N,N-dimethyl-formamide; at 70 ℃; for 22h;

Reference yield: 88.0%

N-hydroxyphthalimide (524-38-9) + 3-methoxybenzyl alcohol (6971-51-3) → 2-[(3-methoxyphenyl)methoxy]-1H-isoindole-1,3(2H)-dione (2014-60-0)

Guidance literature:

With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 20 ℃; for 25h;

DOI:10.1016/S0968-0896(02)00328-0

Reference yield:

N-hydroxyphthalimide (524-38-9) → 2-[(3-methoxyphenyl)methoxy]-1H-isoindole-1,3(2H)-dione (2014-60-0)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.14233/ajchem.2017.20865

upstream raw materials:

N-hydroxyphthalimide

1-bromomethyl-3-methoxybenzene

3-methoxybenzyl alcohol

m-methoxybenzyl chloride

Downstream raw materials:

1-[(aminooxy)methyl]-3-methoxybenzene

C₁₉H₂₅N₃O₄

7-[3-amino-4-(3'-methoxybenzyloxyimino)piperidin-1-yl]-1-cyclopropyl-6-fluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

C₁₈H₂₇N₃O₄

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