1,1'-([2,2'-bipyridine]-4,4'-diylbis(methylene))bis(3-(3,5-bis(triflu-oromethyl)phenyl)-thiourea)

Base Information

• Chemical Name: 1,1'-([2,2'-bipyridine]-4,4'-diylbis(methylene))bis(3-(3,5-bis(triflu-oromethyl)phenyl)-thiourea)
• CAS No.: 1431384-63-2
• Molecular Formula: C₃₀H₂₀F₁₂N₆S₂
• Molecular Weight: 756.642
• Mol file: 1431384-63-2.mol

Synonyms:1,1'-([2,2'-bipyridine]-4,4'-diylbis(methylene))bis(3-(3,5-bis(triflu-oromethyl)phenyl)-thiourea)

Chemical Property of 1,1'-([2,2'-bipyridine]-4,4'-diylbis(methylene))bis(3-(3,5-bis(triflu-oromethyl)phenyl)-thiourea)

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1,1'-([2,2'-bipyridine]-4,4'-diylbis(methylene))bis(3-(3,5-bis(triflu-oromethyl)phenyl)-thiourea)

There total 5 articles about 1,1'-([2,2'-bipyridine]-4,4'-diylbis(methylene))bis(3-(3,5-bis(triflu-oromethyl)phenyl)-thiourea) 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: 85.0%

4,4'-bis(aminomethyl)-2,2'-bipyridine (727380-18-9) + 3,5-bistrifluoromethylphenylisothiocyanate (23165-29-9) → 1,1'-([2,2'-bipyridine]-4,4'-diylbis(methylene))bis(3-(3,5-bis(triflu-oromethyl)phenyl)-thiourea) (1431384-63-2)

Guidance literature:

In chloroform; at 20 ℃; for 6h;

DOI:10.1016/j.tetasy.2013.03.014

Reference yield:

4,4'-bis(carbomethoxy)-2,2'-bipyridine (71071-46-0) → 1,1'-([2,2'-bipyridine]-4,4'-diylbis(methylene))bis(3-(3,5-bis(triflu-oromethyl)phenyl)-thiourea) (1431384-63-2)

Guidance literature:

Multi-step reaction with 4 steps

1: sodium tetrahydroborate / ethanol / Reflux

2: hydrogen bromide / Reflux

3: potassium phtalimide / N,N-dimethyl-formamide

4: chloroform / 6 h / 20 °C

With sodium tetrahydroborate; hydrogen bromide; potassium phtalimide; In ethanol; chloroform; N,N-dimethyl-formamide;

DOI:10.1016/j.tetasy.2013.03.014

Reference yield:

4,4'-bis(hydroxymethyl)-2,2'-bipyridine (109073-77-0) → 1,1'-([2,2'-bipyridine]-4,4'-diylbis(methylene))bis(3-(3,5-bis(triflu-oromethyl)phenyl)-thiourea) (1431384-63-2)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrogen bromide / Reflux

2: potassium phtalimide / N,N-dimethyl-formamide

3: chloroform / 6 h / 20 °C

With hydrogen bromide; potassium phtalimide; In chloroform; N,N-dimethyl-formamide;

DOI:10.1016/j.tetasy.2013.03.014

upstream raw materials:

4,4'-dimethyl-2,2'-bipyridines

2,2'-Bipyridine-4,4'-dicarboxylic acid

4,4'-bis(carbomethoxy)-2,2'-bipyridine

4,4'-bis(hydroxymethyl)-2,2'-bipyridine