1064-74-0

Upstream product

• 4418-61-5 5-aminotetrazole 
• 288-32-4 1H-imidazole 
• 288-13-1 NH-pyrazole 
• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 1455443-28-3 C₁₆H₁₆ClN₂O₃⁽¹⁺⁾*Cl^(1-) 
• 1455443-29-4 C₁₆H₁₆BrN₂O₃⁽¹⁺⁾*Br^(1-) 
• 603-35-0 triphenylphosphine 
• 1451064-28-0 N-vinylisonicotinic acid chloride 
• 45590-51-0 N-vinylpyridinium chloride 
• 1143517-95-6 2-methyl-1-vinylpyridinium chloride 
• 953054-44-9 3,5-dibromo-1-vinylpyridinium chloride 
• 565-64-0 2,3-dichloropropanoic acid 
• 542-58-5 2-chloro-1-acetoxyethane 

Downstream Products

• 194784-33-3 (C₆H₅)3PCH₂CH₂P(C₆H₅)3⁽²⁺⁾*Os₂Cl₈^(2-)=[(C₆H₅)3PCH₂CH₂P(C₆H₅)3][Os₂Cl₈] 

Relevant academic research and scientific papers

Specificity of the reaction of β-carboxyvinyl(triphenyl)phosphonium chloride with azoles

Reactions of pyrazole, 3,5-dimethylpyrazole, 1,2,4-triazole, 5-aminotetrazole, and imidazole with β-carboxyvinyl(triphenyl)phosphonium chloride in boiling acetonitrile are accompanied by elimination of azole with formation of the initial salt and eliminat

Special features of the interaction of pyridine and quinoline derivatives, and related compounds with triphenylphosphine

Using pyridine, quinoline, and related compounds as examples, it has been shown that their interaction with triphenylphosphine occurs via different pathways. Reaction of triphenylphosphine with N-vinylisonicotinic acid chloride leads to the mixture of 1,2

Features of the reaction of 2,3-dihalopropanoic acids with pyridines and nucleophilic addition to N-vinylpyridinium salts

The example of vinylpyridinium salts to establish for the first time the possibility of nucleophilic addition to the vinyl group in quaternary ammonium salts, which provides evidence against the concept that such reactions involve d orbitals. The nucleoph

Reaction of 2,3-dihalopropionic acids and their derivatives with P- and N-nucleophiles

3-(Triphenylphosphoniochlorido)acrylic and 2,3-dichloropropionic acids react with triphenylphosphine to form 1,2-bis(triphenylphosphoniochlorido) ethane. Under analogous conditions, 2,3-dibromopropionic acid undergoes debromination followed by triphenylphosphine addition to give, after water treatment, 3-(triphenylphosphoniobromido)propionic acid. 2,3- Dihalopropionitriles react similarly, providing 3-(triphenylphosphoniohalido) propionitriles. The reaction of 2,3-dibromopropionamide with triphenylphosphine was performed to show that E-(triphenylphosphoniobromido)acrylic acid is capable, by contrast to what was reported previously, of reacting with triphenylphosphine. Pyridine forms with 2,3-dihalopropionic acids vinylpyridinium halides, while the reactions with aliphatic amines gives rise to dehydrohalogenation products.