2,6-Dibutylphenol

Base Information

• Chemical Name: 2,6-Dibutylphenol
• CAS No.: 62083-20-9
• Molecular Formula: C14H22O
• Molecular Weight: 206.328
• DSSTox Substance ID: DTXSID90550620
• Nikkaji Number: J141.410K
• Wikidata: Q82430043
• Mol file: 62083-20-9.mol

Synonyms:2,6-Dibutylphenol;2,6-di-butylphenol;62083-20-9;SCHEMBL201764;DTXSID90550620

Chemical Property of 2,6-Dibutylphenol

Chemical Property:

• XLogP3: 5.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 6
• Exact Mass: 206.167065321
• Heavy Atom Count: 15
• Complexity: 139

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC1=C(C(=CC=C1)CCCC)O

Technology Process of 2,6-Dibutylphenol

There total 4 articles about 2,6-Dibutylphenol 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: 87.0%

C15H24O → 2,6-di-butylphenol (62083-20-9)

Guidance literature:

With boron tribromide; In dichloromethane; at 20 ℃;

DOI:10.1039/d1sc01731d

Reference yield: 79.5%

1-butylene (106-98-9,9003-28-5) + phenol (108-95-2,27073-41-2) → 4-n-butylphenol (1638-22-8) + ortho-butylphenol (3180-09-4) + 2,4-Dibutylphenol (2151-57-7) + 2,6-di-butylphenol (62083-20-9)

Guidance literature:

at 100 ℃; Ion exchange resin catalyst (Rohm & Haas Amberlyst 36 (dry));

Reference yield: 79.0%

cyclohexanone (108-94-1,11119-77-0,9003-41-2,9075-99-4) + butyraldehyde (123-72-8) → 2,6-di-butylphenol (62083-20-9)

Guidance literature:

With zirconocene dichloride; at 150 ℃; for 8h;

DOI:10.1021/jo00256a061

upstream raw materials:

cyclohexanone

butyraldehyde

1-butylene

phenol