2-[2-oxo-2H-6-(4-isopropylphenoxy)acenaphthylen-1-ylidene]-malononitrile

Base Information

• Chemical Name: 2-[2-oxo-2H-6-(4-isopropylphenoxy)acenaphthylen-1-ylidene]-malononitrile
• CAS No.: 1265828-99-6
• Molecular Formula: C₂₄H₁₆N₂O₂
• Molecular Weight: 364.403
• Mol file: 1265828-99-6.mol

Synonyms:2-[2-oxo-2H-6-(4-isopropylphenoxy)acenaphthylen-1-ylidene]-malononitrile

Chemical Property of 2-[2-oxo-2H-6-(4-isopropylphenoxy)acenaphthylen-1-ylidene]-malononitrile

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-[2-oxo-2H-6-(4-isopropylphenoxy)acenaphthylen-1-ylidene]-malononitrile

There total 3 articles about 2-[2-oxo-2H-6-(4-isopropylphenoxy)acenaphthylen-1-ylidene]-malononitrile 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: 93.0%

5‐(4‐isopropylphenoxy)acenaphthylene-1,2‐dione (1265828-86-1) + malononitrile (109-77-3) → 2-[2-oxo-2H-6-(4-isopropylphenoxy)acenaphthylen-1-ylidene]-malononitrile (1265828-99-6)

Guidance literature:

With silica gel; In dichloromethane; acetonitrile; Reflux;

DOI:10.1016/j.bmc.2012.11.008

Reference yield:

5-bromoacenaphthylene-1,2-dione (26254-35-3) → 2-[2-oxo-2H-6-(4-isopropylphenoxy)acenaphthylen-1-ylidene]-malononitrile (1265828-99-6)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

2: acetonitrile / 1 h / Reflux

With potassium carbonate; In N,N-dimethyl-formamide; acetonitrile;

DOI:10.1021/jm101181u

Reference yield:

acenaphthene quinone (82-86-0) → 2-[2-oxo-2H-6-(4-isopropylphenoxy)acenaphthylen-1-ylidene]-malononitrile (1265828-99-6)

Guidance literature:

Multi-step reaction with 3 steps

1: bromine / 60 °C

2: potassium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

3: acetonitrile / 1 h / Reflux

With bromine; potassium carbonate; In N,N-dimethyl-formamide; acetonitrile;

DOI:10.1021/jm101181u

upstream raw materials:

5‐(4‐isopropylphenoxy)acenaphthylene-1,2‐dione

malononitrile

5-bromoacenaphthylene-1,2-dione

acenaphthene quinone

Downstream raw materials:

3-(4-isopropylphenoxy)-8-oxo-8H-acenaphtho[1,2-b]pyrrole-9-carbonitrile

9-(butylamino)-3-(4-isopropylphenoxy)-8H-acenaphtho[1,2-b]pyrrol-8-one

C₂₉H₃₀N₂O₂

3-(4-isopropylphenoxy)-9-(3-phenylpropylamino)-8H-acenaphtho[1,2-b]pyrrol-8-one