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1-[3-Chloro-5-trifluoromethylphenyl]-2,2,2-trifluoroethanone

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1-[3-Chloro-5-trifluoromethylphenyl]-2,2,2-trifluoroethanone Basic information

Product Name:
1-[3-Chloro-5-trifluoromethylphenyl]-2,2,2-trifluoroethanone
Synonyms:
  • 1-[3-Chloro-5-trifluoromethylphenyl]-2,2,2-trifluoroethanone
  • 3'-Chloro-5'-trifluoroMethyl-2,2,2-trifluoroacetophenone
  • 2,2,2-trifluoro-3'-chloro-5'-trifluoromethylacetophenone
  • 3'-Chloro-5'-trifluoromethoxy-2,2,2-trifluoroacetophenone
  • 1-(3-chloro-5-(trifluoromethyl)phenyl)-2,2,2-trifluoroethan-1-one
  • Ethanone, 1-[3-chloro-5-(trifluoromethyl)phenyl]-2,2,2-trifluoro-
  • 1-(3-chloro-5-(trifluoromethyl)phenyl)-2,2,2-trifluoroethan-1-one (Afoxolaner intermediate)
  • 1-[3-Chloro-5-trifluoromethylphenyl]-2,2,2-trifluoroethanone ISO 9001:2015 REACH
CAS:
1125812-58-9
MF:
C9H3ClF6O
MW:
276.56
Mol File:
1125812-58-9.mol
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1-[3-Chloro-5-trifluoromethylphenyl]-2,2,2-trifluoroethanone Chemical Properties

Boiling point:
203℃
Density 
1.512
Flash point:
77℃
storage temp. 
2-8°C
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1-[3-Chloro-5-trifluoromethylphenyl]-2,2,2-trifluoroethanone Usage And Synthesis

Uses

1-[3-Chloro-5-trifluoromethylphenyl]-2,2,2-trifluoroethanone can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.

Synthesis


Cool the solution containing compound III (74.4g, 0.255mol containing compound III) to -100, and add 120g of sulfuric acid with a mass fraction of 92.5% to the above system while keeping the temperature below 0. After acidification, continue to react and keep for 1.5h, and then add 126.7g of 33% sodium nitrite aqueous solution (containing diazotizing reagent sodium nitrite 0.612mol) into the system uniformly within 2h, and keep the temperature at 0 The following reaction is carried out for 2 hours, and the system is heated to room temperature after full reaction, 111.1 g of 50% hypophosphorous acid and 0.67 g of cuprous oxide are added, and the reaction is stirred for 2 hours while keeping temperature. After the reaction is over, stand to separate the layers, and wash the organic layer with a 5% sodium bicarbonate aqueous solution, dry with anhydrous magnesium sulfate, and rectify to obtain a clear and transparent oily liquid 1-[3-chloro-5-(trifluoromethyl) (Yl)phenyl]-2,2,2-trifluoroethanone 66.9, content 99.5%, yield 87.2%.

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