2-chloro-N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine

Base Information

Chemical Name:2-chloro-N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine
CAS No.:128316-04-1
Molecular Formula:C₂₁H₂₄ClNO₂
Molecular Weight:357.88
Hs Code.:

Synonyms:2-chloro-N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine

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Chemical Property of 2-chloro-N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine

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Technology Process of 2-chloro-N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine

There total 4 articles about 2-chloro-N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine 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: 70.0%

: 128316-06-3
2-chloro-4-hydroxy-N-(4-hydroxy-3,5-di-tert-butylbenzylidene)aniline

: 128316-04-1
2-chloro-N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine

Guidance literature:: With lead dioxide; In benzene; at 20 ℃; for 3h;

Reference yield:

: 3964-52-1
2-chloro 4-aminophenol

: 128316-04-1
2-chloro-N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine

Guidance literature:: Multi-step reaction with 2 steps

1: 12.4 g / toluene / 3 h / Heating

2: 70 percent / lead dioxide / benzene / 3 h / 20 °C

With lead dioxide; In toluene; benzene;

Reference yield:

: 122134-52-5
N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine

: 128316-04-1
2-chloro-N-(2,6-di-tert-butyl-1-oxocyclohexa-2,5-dien-4-ylidenemethyl)-1,4-benzoquinone imine

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / HCl / benzene / 20 °C

2: 70 percent / lead dioxide / benzene / 3 h / 20 °C

With hydrogenchloride; lead dioxide; In benzene;