1H-Isoindole-1,3(2H)-dione, 2-[(4-ethenylphenyl)methyl]-

Base Information

• Chemical Name: 1H-Isoindole-1,3(2H)-dione, 2-[(4-ethenylphenyl)methyl]-
• CAS No.: 63413-74-1
• Molecular Formula: C17H13NO2
• Molecular Weight: 263.296
• DSSTox Substance ID: DTXSID80599700
• Nikkaji Number: J999.368A
• Wikidata: Q82495627

Synonyms:63413-74-1;1H-Isoindole-1,3(2H)-dione, 2-[(4-ethenylphenyl)methyl]-;2-(4-vinylbenzyl)isoindoline-1,3-dione;2-[(4-ETHENYLPHENYL)METHYL]ISOINDOLE-1,3-DIONE;2-[(4-Ethenylphenyl)methyl]-1H-isoindole-1,3(2H)-dione;2-[(4-ethenylphenyl)methyl]-2,3-dihydro-1H-isoindole-1,3-dione;N-p-vinylbenzylphthalimide;N-(p-vinylbenzyl) phthalimide;SCHEMBL1638641;DTXSID80599700;ZBJMAORHMHEGKX-UHFFFAOYSA-N;A1-33067

Chemical Property of 1H-Isoindole-1,3(2H)-dione, 2-[(4-ethenylphenyl)methyl]-

Chemical Property:

• XLogP3: 3.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 263.094628657
• Heavy Atom Count: 20
• Complexity: 385

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CC1=CC=C(C=C1)CN2C(=O)C3=CC=CC=C3C2=O

Technology Process of 1H-Isoindole-1,3(2H)-dione, 2-[(4-ethenylphenyl)methyl]-

There total 5 articles about 1H-Isoindole-1,3(2H)-dione, 2-[(4-ethenylphenyl)methyl]- 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: 98.0%

4-Vinylbenzyl chloride (1592-20-7,29296-32-0) + potassium phtalimide (1074-82-4) → 2-(4-ethenylbenzyl)-1H-isoindole-1,3(2H)-dione (63413-74-1)

Guidance literature:

In N,N-dimethyl-formamide;

DOI:10.1002/pola.26584

Reference yield: 88.0%

phthalimide (136918-14-4,85-41-6) + 4-Vinylbenzyl chloride (1592-20-7,29296-32-0) → 2-(4-ethenylbenzyl)-1H-isoindole-1,3(2H)-dione (63413-74-1)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 25 ℃; Schlenk technique; Inert atmosphere;

DOI:10.1021/acs.orglett.8b00023

Reference yield:

4-((1,3-dioxoisoindolin-2-yl)methyl)benzaldehyde (51359-79-6) + Methylenetriphenylphosphorane (19493-09-5) → 2-(4-ethenylbenzyl)-1H-isoindole-1,3(2H)-dione (63413-74-1)

Guidance literature:

In tetrahydrofuran; at 0 - 20 ℃; for 1.5h;

upstream raw materials:

4-Vinylbenzyl chloride

potassium phtalimide

phthalimide

4-((1,3-dioxoisoindolin-2-yl)methyl)benzaldehyde

Downstream raw materials:

p-vinylbenzylamine

C₃₂H₃₀N₂O₅S

C₂₅H₂₃NO₆S

C₁₈H₁₆FNO₃

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