14377-99-2

Upstream product

• 6114-57-4 (Z)-2,3-diphenylacrylonitrile 
• 100-47-0 benzonitrile 
• 140-29-4 phenylacetonitrile 
• 100-52-7 benzaldehyde 

Downstream Products

• 127679-78-1 methyl (2S,4R)-2,3,4-triphenylpentanedioate 
• 127680-16-4 5-(4-methoxy-1-naphthyl)-5-oxo-2,3,4-triphenylpentanoic acid 
• 127680-14-2 5-(3,4-dimethoxyphenyl)-5-oxo-2,3,4-triphenylpentanoic acid 
• 127680-15-3 5-(4-ethoxyphenyl)-5-oxo-2,3,4-triphenylpentanoic acid 
• 127680-11-9 ((1R,2R)-3-Oxo-2-phenyl-indan-1-yl)-phenyl-acetic acid methyl ester 
• 127680-10-8 2,3-dihydro-1-oxo-2,α-diphenyl-1H-indene-3-acetic acid 
• 127680-09-5 2,3,4-triphenylpentanedioic anhydride 
• 127680-08-4 (2S,4R) 2,3,4-triphenylpentanedioic acid 
• 127680-09-5 2,3,4-triphenyl-glutaric acid-anhydride 
• 74-90-8 hydrogen cyanide 
• 64-04-0 phenethylamine 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 127680-08-4 2,3,4-triphenyl-glutaric acid 
• 16610-80-3 (E)-2,3-diphenylacrylonitrile 

Relevant academic research and scientific papers

Solvent-free condensation of arylacetonitrile with aldehydes

The condensation of a series of arylacetonitriles with aldehydes can be carried out by mixing equivalent amounts of reagents with neat powdered KOH at room temperature for 3-60 min depending on the aldehyde steric hindrance. At higher temperature (110°C), yields were generally higher and purity increased within very short reaction times (1-5 min). With pentamethylphenylacetonitrile, a phase transfer agent was necessary to give a satisfactory yield.

Water-soluble calixarenes as new inverse phase-transfer catalysts. Their application to aldol-type condensation and Michael addition reactions in water

Aldol-type condensation and Michael addition reactions of activated methyl and methylene compounds in aqueous NaOH solution have been developed without the need for any added organic solvents. The water-soluble calix[n]arenes, which contain trimethylammon