1190865-44-1

Basic information

• Product Name: 1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone
• Synonyms: 1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone;2,2,2-Trifluoro-3',5'-dichloro-4'-fluoroacetophenone
• CAS NO: 1190865-44-1
• Molecular Formula: C8H2Cl2F4O
• Molecular Weight: 261.0004928
• EINECS: -0
• Mol File: 1190865-44-1.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 282.5±40.0 °C(Predicted)
• Appearance: /
• Density: 1.577±0.06 g/cm3(Predicted)
• Vapor Pressure: 20-2750Pa at 20-37.8℃
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone(1190865-44-1)
• EPA Substance Registry System: 1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone(1190865-44-1)

Safety Data

• Hazardous Substances Data: 1190865-44-1(Hazardous Substances Data)

Usage

Uses

1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone can be used as a pesticide intermediate, mainly in the synthesis of sarolaner.

Upstream product

• 383-63-1 ethyl trifluoroacetate, 
• 133307-08-1 1,3-dichloro-2-fluoro-5-iodo-benzene 
• 2729-34-2 3,5-dichloro-4-fluorophenylamine 
• 655-32-3 2,2,2-trifluoro-1-(4-fluorophenyl)ethanone 
• 431-47-0 trifluoroacetic acid-methyl ester 
• 17318-08-0 5-bromo-1,3-dichloro-2-fluorobenzene 
• 81290-20-2 (trifluoromethyl)trimethylsilane 
• 697-88-1 4-bromo-2,6-dichloroaniline 
• 21928-51-8 5-bromo-1,2,3-trichloro-benzene 
• 104863-67-4 N-methoxy-N-methyltrifluoroacetamide 
• 462-06-6 fluorobenzene 
• 340-07-8 N-(trifluoroacetyl)piperidine 
• 158401-00-4 1-(3,4,5-trichloro-phenyl)-2,2,2-trifluoro-ethanone 
• 1297553-45-7 2,2,2-trifluoro-1-(4-fluoro-3-nitrophenyl)ethan-1-one 

Downstream Products

• 1414377-96-0 3-[3-(3,5-dichloro-4-fluoro-phenyl)-4,4,4-trifluoro-3-hydroxy-butyryl]-5,6-dihydro-4H-cyclopenta[c]thiophene-1-carboxylic acid methyl ester 
• 1575811-25-4 tert-butyl 5'-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-1,4,2-dioxazol-3-yl)-3'H-spiro[azetidine-3,1'-isobenzofuran]-1-carboxylate 
• 1398610-04-2 tert-butyl 6-[(E/Z)-3-(3,5-dichloro-4-fluoro-phenyl)-4,4,4-trifluoro-but-2-enoyl]spiro[1H-isobenzofuran-3,3'-azetidine]-1'-carboxylate 

Relevant articles and documents

METHOD FOR PREPARING 3,5-DIHALOTRIFLUOROACETOPHENONE AND DERIVATIVE THEREOF

The present application relates to the technical field of chemical pharmacy, and in particular, to a method for preparing 3,5-dihalotrifluoroacetophenone and a derivative thereof. 3-halogen-4-nitrotrifluoroacetophenone is used as a raw material, and the 3,5-dihalotrifluoroacetophenone derivative is finally obtained by means of a reduction reaction, a halogenation reaction and an amino substitution reaction. The raw material thereof is cheap and easily available, the process is simple, the conditions are mild, and the method has the prospect of large-scale production and has good economic effects.

Preparation method of halogenated trifluoroacetyl benzene

The invention relates to the field of organic synthesis, in particular to a preparation method of halogenated trifluoroacetyl benzene. The invention provides a preparation method of 3,4,5-trichlorotrifluoroacetyl benzene on the first aspect, which comprises the following steps: 1) carrying out diazotization and chlorination reaction on 2,6-dichloro-4-bromoaniline to provide 3,4,5-trichlorobromobenzene; (2) carrying out Grignard reaction on the 3,4,5-trichlorobromobenzene so as to provide 3,4,5-trichlorophenyl magnesium bromide; and 3) carrying out a trifluoroacetylation reaction on the 3,4,5-trichlorophenyl magnesium bromide and a trifluoroacetylation reagent, so as to provide the 3,4,5-trichlorotrifluoroacetyl benzene. According to the preparation method of 3,4,5-trichlorotrifluoroacetyl benzene, provided by the invention, 2,6-dichloro-4-bromoaniline is adopted as a raw material, a target product is prepared through a diazotization reaction, a Grignard reaction and a trifluoroacetylation reaction, the whole preparation route is simple in reaction step operation, the product is easy to purify, the yield is high, and the preparation method is very suitable for large-scale production; and the method has a good industrialization prospect.

Preparation method of trifluoroacetophenone derivative

The invention relates to the field of organic synthesis, in particular to a preparation method of a trifluoroacetophenone derivative. Substituted aniline is used as a raw material, and preparation of the trifluoroacetophenone derivative is completed through three steps including diazotization reaction, coupling reaction and hydrolysis reaction. The preparation method has the advantages of simple process, high yield and less three wastes generated by the whole reaction, and is suitable for large-scale industrial production.