113138-61-7

Upstream product

• 559-91-1 1-phenylperfluorobutan-1-one 
• 2303-76-6 sodium diethyl phosphite 

Downstream Products

• 117482-41-4 5-Fluoro-4-phenyl-6-trifluoromethyl-pyrimidin-2-ylamine 
• 117482-40-3 5-Fluoro-2,4-diphenyl-6-trifluoromethyl-pyrimidine 
• 125742-03-2 2-fluoro-3-hydroxy-2-(1,1,2,2,2-pentafluoroethyl)-1,3-diphenyl-1-propanone 
• 125742-03-2 2-fluoro-3-hydroxy-2-(1,1,2,2,2-pentafluoroethyl)-1,3-diphenyl-1-propanone 
• 113138-62-8 2-(diethylmalono)-F-1-propenyl phenyl ketone 
• 117482-44-7 4-Fluoro-1-methyl-5-phenyl-3-trifluoromethyl-1H-pyrazole 
• 114288-01-6 2-Fluoro-3-hydroxy-4-methyl-2-pentafluoroethyl-1-phenyl-pentan-1-one 
• 114288-01-6 2-fluoro-3-hydroxy-4-methyl-2-(1,1,2,2,2-pentafluoroethyl)-1-phenyl-1-pentanone 
• 114288-01-6 2-fluoro-3-hydroxy-4-methyl-2-(1,1,2,2,2-pentafluoroethyl)-1-phenyl-1-pentanone 
• 114288-00-5 2-Fluoro-3-hydroxy-2-pentafluoroethyl-1-phenyl-hexan-1-one 
• 114288-00-5 2-fluoro-3-hydroxy-2-(1,1,2,2,2-pentafluoroethyl)-1-phenyl-1-hexanone 
• 114288-00-5 2-fluoro-3-hydroxy-2-(1,1,2,2,2-pentafluoroethyl)-1-phenyl-1-hexanone 
• 113487-31-3 2,3,3,4,4,4-hexafluoro-1-phenyl-1-butanone 
• 125742-06-5 1-phenyl-(2E)-2,3,4,4,4-pentafluorobut-2-en-1-ol 

Relevant academic research and scientific papers

A NEW EFFICIENT METHOD FOR THE GENERATION OF F-ALKYL KETONE METAL ENOLATES BY USING COPPER(II) BROMIDE-LITHIUM ALUMINIUM HYDRIDE REAGENT AND THEIR ALDOL REACTION WITH CARBONYL COMPOUNDS

1-Substituted F-1-alkenyl phosphates, readily prepared from F-alkyl ketones end sodium diethyl phosphite, were treated with copper(II) bromide-lithium aluminium hydride reagent at -30 degC to generate in situ F-alkyl ketone aluminium enolates, which under

A New Effective and Convenient Route to Fluorinated Nitrogen Heterocyclic Compounds by the Use of Enol Phosphates Derived from F-Alkyl Ketones

The treatment of F-alkyl ketones with sodium diethyl phosphite in tetrahydrofuran at -10 to 0 deg C gave high yields of 1-substituted F-1-alkenyl phosphates, which readily reacted with amidine of hydrazine derivatives at room temperature to afford the cor