1-(3-Chloro-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide

Base Information

• Chemical Name: 1-(3-Chloro-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide
• CAS No.: 76950-81-7
• Molecular Formula: C₂₅H₂₁ClNS*I
• Molecular Weight: 529.872
• Mol file: 76950-81-7.mol

Synonyms:1-(3-Chloro-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide

Chemical Property of 1-(3-Chloro-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 1-(3-Chloro-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide

There total 3 articles about 1-(3-Chloro-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide 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: 92.0%

1-(3-Chloro-benzyl)-4,6-diphenyl-1H-pyridine-2-thione (76950-88-4) + methyl iodide (74-88-4) → 1-(3-Chloro-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide (76950-81-7)

Guidance literature:

In benzene; Ambient temperature;

DOI:10.1055/s-1980-29239

Reference yield:

4,6-diphenyl-2H-pyran-2-thione (26479-00-5) → 1-(3-Chloro-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide (76950-81-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 72 percent / methanol / 3 h / Heating

2: 92 percent / benzene / Ambient temperature

In methanol; benzene;

DOI:10.1055/s-1980-29239

Reference yield:

m-chlorobenzylamine (4152-90-3) → 1-(3-Chloro-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide (76950-81-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 72 percent / methanol / 3 h / Heating

2: 92 percent / benzene / Ambient temperature

In methanol; benzene;

DOI:10.1055/s-1980-29239

upstream raw materials:

1-(3-Chloro-benzyl)-4,6-diphenyl-1H-pyridine-2-thione

methyl iodide

4,6-diphenyl-2H-pyran-2-thione

m-chlorobenzylamine

Downstream raw materials:

(3-chlorobenzyl)phosphonic acid ethyl ester

2-Methylthio-4,6-diphenylpyridine

1-Chloro-3-nitrooxymethyl-benzene

1-chloro-3-(iodomethyl)benzene