4,4,4-Trifluoro-1-phenylbutan-1-one

Base Information

• Chemical Name: 4,4,4-Trifluoro-1-phenylbutan-1-one
• CAS No.: 713-02-0
• Molecular Formula: C10H9F3O
• Molecular Weight: 202.176
• DSSTox Substance ID: DTXSID30543713
• Nikkaji Number: J774.210J
• Mol file: 713-02-0.mol

Synonyms:4,4,4-trifluoro-1-phenylbutan-1-one;713-02-0;3-trifluoromethylpropiophenone;SCHEMBL2201165;DTXSID30543713;IRWRIGHYGSXWOL-UHFFFAOYSA-N;MFCD02250289;AKOS003612173;4,4,4-trifluoro-1-phenyl-1-butanone;4,4,4-Trifluoro-1-phenyl-butan-1-one;CS-0236635;EN300-1721009;A866468;Z1235985184

Chemical Property of 4,4,4-Trifluoro-1-phenylbutan-1-one

Chemical Property:

• XLogP3: 3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 202.06054939
• Heavy Atom Count: 14
• Complexity: 192

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(=O)CCC(F)(F)F

Technology Process of 4,4,4-Trifluoro-1-phenylbutan-1-one

There total 35 articles about 4,4,4-Trifluoro-1-phenylbutan-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: 95.0%

(2,2-difluorocyclopropyl)(phenyl)methanone → 1-phenyl-4,4,4-trifluoro-1-butanone (713-02-0)

Guidance literature:

With boron trifluoride diethyl etherate; In chloroform; at 60 ℃; Reagent/catalyst; Solvent; Temperature; Concentration;

DOI:10.1039/c3cc47879c

Reference yield: 90.0%

iodotrifluoromethane (2314-97-8,263005-66-9) + 1-Phenyl-2-propyn-1-ol (4187-87-5) → 1-phenyl-4,4,4-trifluoro-1-butanone (713-02-0)

Guidance literature:

With tris(2,2'-bipyridyl)ruthenium dichloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In N,N-dimethyl-formamide; at 20 ℃; for 24h; Reagent/catalyst; Solvent; Irradiation;

Reference yield: 87.0%

2-chloro-4,4,4-trifluoro-1-phenylbutan-1-one → 1-phenyl-4,4,4-trifluoro-1-butanone (713-02-0)

Guidance literature:

With acetic acid; zinc; In dimethyl sulfoxide; at 20 ℃; Schlenk technique; Glovebox; Inert atmosphere;

DOI:10.1002/cjoc.201900221

upstream raw materials:

2,4,6-trimethyl-pyridine

1-styrenyloxytrimethylsilane

(2,2,2-trifluoroethyl)phenyliodonium triflate

3-chloro-4,4,4-trifluoro-1-phenyl-2-buten-1-one

Downstream raw materials:

C₁₀H₁₂F₃N

6-(ethyloxy)-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

6-bromo-3-methyl-2-(3-trifluoromethyl-phenyl)-quinoline-4-carboxylic acid