3,5-Di-tert-butyl-N-(3,5-di-tert-butyl-4-oxo-cyclohexa-2,5-dienylidene)-4-oxo-cyclohexa-2,5-dienecarboximidic acid 2,4,6-tri-tert-butyl-phenyl ester

Base Information

• Chemical Name: 3,5-Di-tert-butyl-N-(3,5-di-tert-butyl-4-oxo-cyclohexa-2,5-dienylidene)-4-oxo-cyclohexa-2,5-dienecarboximidic acid 2,4,6-tri-tert-butyl-phenyl ester
• CAS No.: 40095-31-6
• Molecular Formula: C₄₇H₆₉NO₃
• Molecular Weight: 696.07
• Mol file: 40095-31-6.mol

Synonyms:

Chemical Property of 3,5-Di-tert-butyl-N-(3,5-di-tert-butyl-4-oxo-cyclohexa-2,5-dienylidene)-4-oxo-cyclohexa-2,5-dienecarboximidic acid 2,4,6-tri-tert-butyl-phenyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3,5-Di-tert-butyl-N-(3,5-di-tert-butyl-4-oxo-cyclohexa-2,5-dienylidene)-4-oxo-cyclohexa-2,5-dienecarboximidic acid 2,4,6-tri-tert-butyl-phenyl ester

There total 4 articles about 3,5-Di-tert-butyl-N-(3,5-di-tert-butyl-4-oxo-cyclohexa-2,5-dienylidene)-4-oxo-cyclohexa-2,5-dienecarboximidic acid 2,4,6-tri-tert-butyl-phenyl 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:

C47H71NO3 (40095-30-5) → 3,5-Di-tert-butyl-N-(3,5-di-tert-butyl-4-oxo-cyclohexa-2,5-dienylidene)-4-oxo-cyclohexa-2,5-dienecarboximidic acid 2,4,6-tri-tert-butyl-phenyl ester (40095-31-6)

Guidance literature:

With potassium hydroxide; potassium hexacyanoferrate(III); In benzene;

Reference yield:

2,4,6-tri-tert-butylphenoxol (732-26-3) → 3,5-Di-tert-butyl-N-(3,5-di-tert-butyl-4-oxo-cyclohexa-2,5-dienylidene)-4-oxo-cyclohexa-2,5-dienecarboximidic acid 2,4,6-tri-tert-butyl-phenyl ester (40095-31-6)

Guidance literature:

Multi-step reaction with 4 steps

1: (i) K₃, aq. KOH, benzene, (ii) /BRN= 4145073/

2: KI, AcOH / benzene

3: 150 - 160 °C

4: K₃, aq. KOH / benzene

With potassium hydroxide; acetic acid; potassium iodide; potassium hexacyanoferrate(III); In benzene;

Reference yield:

C51H79NO3 (40095-29-2) → 3,5-Di-tert-butyl-N-(3,5-di-tert-butyl-4-oxo-cyclohexa-2,5-dienylidene)-4-oxo-cyclohexa-2,5-dienecarboximidic acid 2,4,6-tri-tert-butyl-phenyl ester (40095-31-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 150 - 160 °C

2: K₃, aq. KOH / benzene

With potassium hydroxide; potassium hexacyanoferrate(III); In benzene;

upstream raw materials:

C₄₇H₇₁NO₃

2,4,6-tri-tert-butylphenoxol

C₅₁H₇₉NO₃

C₅₁H₇₈NO₃