4--4-methyl-2,5-cyclohexadienone N-benzoylimine

Base Information

Chemical Name:4--4-methyl-2,5-cyclohexadienone N-benzoylimine
CAS No.:151965-63-8
Molecular Formula:C₂₈H₂₄N₂O₂
Molecular Weight:420.511
Hs Code.:

4-<N-Benzoyl-N-(4-methylphenyl)amino>-4-methyl-2,5-cyclohexadienone N-benzoylimine

Synonyms:4--4-methyl-2,5-cyclohexadienone N-benzoylimine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4--4-methyl-2,5-cyclohexadienone N-benzoylimine

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Technology Process of 4--4-methyl-2,5-cyclohexadienone N-benzoylimine

There total 2 articles about 4--4-methyl-2,5-cyclohexadienone N-benzoylimine 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: 34.0%

: 67-56-1
methanol

: 582-78-5
N-(4-methylphenyl)benzamide

: 4-O-Methyl-4-methyl-p-benzoquinol N-benzoylimine

: 151965-63-8
4--4-methyl-2,5-cyclohexadienone N-benzoylimine

Guidance literature:: With sodium hydrogencarbonate; In water; at 25 ℃; Product distribution; single-cell anodic oxidation, platinum electrodes, a constant current 0.15 A, 10percent LiClO₄ as supporting electrolyte; other temperatures, current densities, supporting electrolyte concentrations;
DOI:10.1021/jo00073a016

Reference yield: 17.0%

: 582-78-5
N-(4-methylphenyl)benzamide

: 4-O-Methyl-4-methyl-p-benzoquinol N-benzoylimine

: 151965-63-8
4--4-methyl-2,5-cyclohexadienone N-benzoylimine

Guidance literature:: With sodium hydrogencarbonate; In methanol; water; at 40 ℃; for 2.5h; single-cell anodic oxidation, platinum electrodes, a constant current 0.15 A, 2percent LiClO₄ as supporting electrolyte;
DOI:10.1021/jo00073a016