4-Methoxy-4-methyl-1-phenyloct-2-YN-1-one

Base Information

• Chemical Name: 4-Methoxy-4-methyl-1-phenyloct-2-YN-1-one
• CAS No.: 84022-51-5
• Molecular Formula: C16H20O2
• Molecular Weight: 244.334
• DSSTox Substance ID: DTXSID60518712
• Mol file: 84022-51-5.mol

Synonyms:4-METHOXY-4-METHYL-1-PHENYLOCT-2-YN-1-ONE;84022-51-5;DTXSID60518712

Chemical Property of 4-Methoxy-4-methyl-1-phenyloct-2-YN-1-one

Chemical Property:

• XLogP3: 3.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 244.146329876
• Heavy Atom Count: 18
• Complexity: 328

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC(C)(C#CC(=O)C1=CC=CC=C1)OC

Technology Process of 4-Methoxy-4-methyl-1-phenyloct-2-YN-1-one

There total 1 articles about 4-Methoxy-4-methyl-1-phenyloct-2-YN-1-one 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: 88.1%

benzoyl chloride (98-88-4) + 3-Methoxy-3-methyl-hept-1-yne → 4-methyl-4-methoxy-1-phenyl-2-octyn-1-one (84022-51-5)

Guidance literature:

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In benzene;

DOI:10.1007/BF00954306

Reference yield: 96.0%

4-methyl-4-methoxy-1-phenyl-2-octyn-1-one (84022-51-5) → 3-amino-4-methyl-4-methoxy-1-phenyl-2-octen-1-one (84598-93-6)

Guidance literature:

With ammonia; In ethanol; at 60 ℃;

DOI:10.1007/BF00955840

Reference yield:

4-methyl-4-methoxy-1-phenyl-2-octyn-1-one (84022-51-5) → 4-methyl-4-methoxy-1-phenyl-1,3-octanediol (84022-36-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 96 percent / ammonia / ethanol / 60 °C

2: 90.5 percent / aq. HCl / ethanol / 3 h / 60 °C

3: 86.2 percent / NaBH₄

With hydrogenchloride; sodium tetrahydroborate; ammonia; In ethanol;

DOI:10.1007/BF00955840

upstream raw materials:

benzoyl chloride

Downstream raw materials:

3-amino-4-methyl-4-methoxy-1-phenyl-2-octen-1-one

4-methyl-4-methoxy-1-phenyl-1,3-octanediol

4-methyl-4-methoxy-1-phenyl-1,3-octanedione