N,N-diphenyl-p-methoxyphenylchloromethyleniminium chloride

Base Information

Chemical Name:N,N-diphenyl-p-methoxyphenylchloromethyleniminium chloride
CAS No.:85121-13-7
Molecular Formula:C₂₀H₁₇ClNO*Cl
Molecular Weight:358.267
Hs Code.:

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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 N,N-diphenyl-p-methoxyphenylchloromethyleniminium chloride

Chemical Property:

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Technology Process of N,N-diphenyl-p-methoxyphenylchloromethyleniminium chloride

There total 1 articles about N,N-diphenyl-p-methoxyphenylchloromethyleniminium chloride 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:

: 16034-40-5
N-(4-Methoxybenzoyl)-diphenylamine

: 85121-13-7
N,N-diphenyl-p-methoxyphenylchloromethyleniminium chloride

Guidance literature:: With oxalyl dichloride; In 1,2-dichloro-ethane; at 60 ℃; for 14h;
DOI:10.1016/S0040-4039(00)85572-0

Reference yield:

: 16577-51-8
hexanoic acid Li-salt

: 85121-13-7
N,N-diphenyl-p-methoxyphenylchloromethyleniminium chloride

: [Hexanoyloxy-(4-methoxy-phenyl)-methylene]-diphenyl-ammonium; chloride

Guidance literature:: In tetrahydrofuran; methanol; at -30 ℃; for 1h;
DOI:10.1016/S0040-4039(00)85572-0

Reference yield:

: 3277-89-2
phenethylmagnesium bromide

: 16577-51-8
hexanoic acid Li-salt

: 85121-13-7
N,N-diphenyl-p-methoxyphenylchloromethyleniminium chloride

: 6047-99-0
1-phenyloctan-3-one

: [Hexanoyloxy-(4-methoxy-phenyl)-methylene]-diphenyl-ammonium; chloride

Guidance literature:: copper(l) iodide; In tetrahydrofuran; dichloromethane; Product distribution; Mechanism; One-pot synthesis of ketones from carboxylic acids (salts) and Grignard reagents using methyleneiminium salts as condensation reagents;
DOI:10.1016/S0040-4039(00)85572-0