1-Methyl-4-((3-methylbut-2-en-1-yl)oxy)benzene

Base Information

• Chemical Name: 1-Methyl-4-((3-methylbut-2-en-1-yl)oxy)benzene
• CAS No.: 23446-54-0
• Molecular Formula: C12H16O
• Molecular Weight: 176.258
• DSSTox Substance ID: DTXSID50536960
• Nikkaji Number: J966.858F
• Mol file: 23446-54-0.mol

Synonyms:1-methyl-4-((3-methylbut-2-en-1-yl)oxy)benzene;1-Methyl-4-[(3-methylbut-2-en-1-yl)oxy]benzene;23446-54-0;SCHEMBL14012896;DTXSID50536960;NMLCTZQTLIPTLX-UHFFFAOYSA-N;p-methylphenoxy-3-methylbut-2-ene;AKOS008952404

Chemical Property of 1-Methyl-4-((3-methylbut-2-en-1-yl)oxy)benzene

Chemical Property:

• XLogP3: 3.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 176.120115130
• Heavy Atom Count: 13
• Complexity: 160

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)OCC=C(C)C

Technology Process of 1-Methyl-4-((3-methylbut-2-en-1-yl)oxy)benzene

There total 12 articles about 1-Methyl-4-((3-methylbut-2-en-1-yl)oxy)benzene 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: 90.0%

p-cresol (106-44-5) + 3-methyl-2-buten-1-ol (556-82-1) → 2,2,6-trimethyl-3,4-dihydro-2H-chromene (23446-57-3) + 3-methyl-1-(3-methylbut-2-enyloxy)but-2-ene (26902-25-0) + 4-methyl-2-(3-methyl-2-buten-1-yl)phenol (23446-56-2) + 1-methyl-4-(3-methylbut-2-enyloxy)benzene (23446-54-0)

Guidance literature:

With Zeolites ZSM; In n-heptane; at 100 ℃; for 10h;

DOI:10.1134/S1070363220030032

Reference yield: 90.0%

p-cresol (106-44-5) + prenyl bromide (870-63-3) → 1-methyl-4-(3-methylbut-2-enyloxy)benzene (23446-54-0)

Guidance literature:

With potassium carbonate; In acetone; at 60 ℃; for 16h;

DOI:10.1016/j.tet.2010.01.048

Reference yield: 47.0%

p-cresol (106-44-5) + 3-methyl-2-buten-1-ol (556-82-1) → 2,2,6-trimethyl-3,4-dihydro-2H-chromene (23446-57-3) + 3-methyl-1-(3-methylbut-2-enyloxy)but-2-ene (26902-25-0) + 4-methyl-2-(3-methyl-2-buten-1-yl)phenol (23446-56-2) + 1-methyl-4-(3-methylbut-2-enyloxy)benzene (23446-54-0) + 2,6-bis(2-methylbut-3-en-2-yl)-4-methylphenol + 2,6-bis(3-methylbut-2-en-1-yl)-4-methylphenol (82719-55-9)

Guidance literature:

With Zeolites ZSM; In n-heptane; at 100 ℃; for 5h;

DOI:10.1134/S1070363220030032

upstream raw materials:

sodium 4-methylphenoxide

prenyl bromide

p-cresol

3,3-dimethyl-allyl chloride

Downstream raw materials:

isopentyl-p-tolyl ether

p-cresol

trimethyl(4-methyl-2-(2-methylbut-3-en-2-yl)phenoxy)silane

Acetic acid 2-(1,1-dimethyl-5-oxo-hexyl)-4-methyl-phenyl ester

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