4,4-Diphenyl-1-butyliodide

Base Information

• Chemical Name: 4,4-Diphenyl-1-butyliodide
• CAS No.: 169756-94-9
• Molecular Formula: C₁₆H₁₇I
• Molecular Weight: 336.215
• Mol file: 169756-94-9.mol

Synonyms:4,4-Diphenyl-1-butyliodide

Chemical Property of 4,4-Diphenyl-1-butyliodide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4,4-Diphenyl-1-butyliodide

There total 6 articles about 4,4-Diphenyl-1-butyliodide 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: 67.0%

4-methanesulfonyloxy-1,1-diphenylbutane (104675-46-9) → 4,4-Diphenyl-1-butyliodide (169756-94-9)

Guidance literature:

Reference yield:

1,1-diphenyl-4-bromobutane (36265-55-1) → 4,4-Diphenyl-1-butyliodide (169756-94-9)

Guidance literature:

With sodium iodide; In diethyl ether; butanone;

Reference yield:

4,4-diphenyl-1-butanol (56740-71-7) → 4,4-Diphenyl-1-butyliodide (169756-94-9)

Guidance literature:

With 1H-imidazole; triphenylphosphine diiodide; In dichloromethane; Ambient temperature;

DOI:10.1021/jm970497w

upstream raw materials:

4,4-diphenyl-1-butanol

4-hydroxy-4,4-diphenylbutyl chloride

bromobenzene

1,1-diphenyl-4-bromobutane

Downstream raw materials:

4,4-diphenyl-1-butyl azide

4,4-Diphenylbutylamine

[[2-(4,4-Diphenylbutyl)thio-4,5-dihydronaphtho[1,2-d]thiazol-6-yl]oxy]acetic Acid

[[2-(4,4-Diphenylbutyl)sulfonyl-4,5-dihydronaphtho[1,2-d]thiazol-6-yl]oxy]acetic Acid

Refernces

• 1、 -. "Tricyclic compounds, their production and use". . . Retrieved 2008/06/13.
• 2、 Ornstein, Paul L.,Bleisch, Thomas J.,Arnold, M. Brian,Wright, Rebecca A.,Johnson, Bryan G.,Schoepp, Darryle D.. "2-substituted-(2SR)-2-amino-2-((1SR,2SR)-2-carboxycycloprop-1- yl)glycines as potent and selective antagonists of group II metabotropic glutamate receptors. 1. Effects of alkyl, arylalkyl, and diarylalkyl substitution". . p. 346 - 357. Retrieved 2007/10/03.