3-Benzoyl-2-methylquinolin-4(1H)-one

Base Information

• Chemical Name: 3-Benzoyl-2-methylquinolin-4(1H)-one
• CAS No.: 109093-22-3
• Molecular Formula: C17H13NO2
• Molecular Weight: 263.296
• DSSTox Substance ID: DTXSID00551340
• Wikidata: Q82430947
• Mol file: 109093-22-3.mol

Synonyms:109093-22-3;3-Benzoyl-2-methylquinolin-4(1H)-one;SCHEMBL14194486;DTXSID00551340

Chemical Property of 3-Benzoyl-2-methylquinolin-4(1H)-one

Chemical Property:

• XLogP3: 3.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 263.094628657
• Heavy Atom Count: 20
• Complexity: 446

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C(=O)C2=CC=CC=C2N1)C(=O)C3=CC=CC=C3

Technology Process of 3-Benzoyl-2-methylquinolin-4(1H)-one

There total 12 articles about 3-Benzoyl-2-methylquinolin-4(1H)-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:

3-benzyl-2-methylquinolin-4-ol (1151-39-9) → (4-hydroxy-2-methyl-quinolin-3-yl)-phenyl-methanone (109093-22-3)

Guidance literature:

With chromium(VI) oxide; acetic acid; at 70 ℃;

DOI:10.1021/ja01604a042

Reference yield:

2-methylquinolin-4-yl benzoate (111947-01-4) → (4-hydroxy-2-methyl-quinolin-3-yl)-phenyl-methanone (109093-22-3)

Guidance literature:

With aluminium trichloride; at 200 ℃;

DOI:10.1021/ja01604a042

Reference yield:

aniline (62-53-3) → (4-hydroxy-2-methyl-quinolin-3-yl)-phenyl-methanone (109093-22-3)

Guidance literature:

Multi-step reaction with 2 steps

2: diphenyl ether

With diphenylether;

upstream raw materials:

4-hydroxy-2-methylquinoline

benzoyl chloride

3-benzyl-2-methylquinolin-4-ol

2-methylquinolin-4-yl benzoate

Downstream raw materials:

(4-methoxy-2-methyl-[3]quinolyl)-phenyl ketone

(4-chloro-2-methyl-[3]quinolyl)-phenyl ketone