31466-31-6

Basic information

• Product Name: 1-Pyrrolidineacetonitrile, a-phenyl-
• CAS NO: 31466-31-6
• Molecular Formula: C12H14N2
• Molecular Weight: 186.257
• Mol File: 31466-31-6.mol
• Article Data: 32

Chemical Properties

• CAS DataBase Reference: 1-Pyrrolidineacetonitrile, a-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pyrrolidineacetonitrile, a-phenyl-(31466-31-6)
• EPA Substance Registry System: 1-Pyrrolidineacetonitrile, a-phenyl-(31466-31-6)

Safety Data

• Hazardous Substances Data: 31466-31-6(Hazardous Substances Data)

Upstream product

• 532-28-5 (RS)-mandelonitrile 
• 609-36-9 rac-Pro-OH 
• 123-75-1 pyrrolidine 
• 100-52-7 benzaldehyde 
• 7677-24-9 trimethylsilyl cyanide 
• 100-51-6 benzyl alcohol 
• 557-21-1 zinc(II) cyanide 
• 623-49-4 ethyl cyanoformate 
• 147-85-3 L-proline 
• 143-33-9 sodium cyanide 
• 477531-68-3 C₉H₁₆BN₃ 
• 2942-58-7 diethyl cyanophosphonate 
• 151-50-8 potassium cyanide 
• 29897-82-3 N-benzylpyrrolidine 

Downstream Products

• 110148-11-3 1-(1,4-diphenyl-butyl)-pyrrolidine 
• 31788-79-1 2-Phenyl-2-pyrrolidinoacetamid 
• 106165-52-0 3-pyrrolidin-1-yl-3-phenylprop-1-ene 
• 3389-54-6 n-benzoylpyrrolidine 
• 1025-56-5 N-benzyl-2-phenyl-pyrrolidine 
• 72219-09-1 1-benzylpyrrolidine-2-carbonitrile 
• 120153-68-6 N-benzylpiperidine-2-carbonitrile 
• 495-71-6 phenacylacetophenone 
• 4441-01-4 1,2,4-triphenylbutane-1,4-dione 
• 108897-21-8 1-(1-phenyl-but-2ξ-enyl)-pyrrolidine 
• 101132-02-9 1-((E)-1-Phenyl-but-2-enyl)-pyrrolidine 
• 110150-82-8 1-(1,3-diphenyl-butyl)-pyrrolidine 
• 116858-53-8 C₂₄H₂₈N₂ 
• 116858-50-5 (Z)-2,3,5-Triphenyl-2,5-di-pyrrolidin-1-yl-pent-4-enenitrile 

Relevant articles and documents

Ruthenium and Iron-Catalysed Decarboxylative N-alkylation of Cyclic Α-Amino Acids with Alcohols: Sustainable Routes to Pyrrolidine and Piperidine Derivatives

A modular and waste-free strategy for constructing N-substituted cyclic amines via decarboxylative N-alkylation of α-amino acids employing ruthenium- and iron-based catalysts is presented. The reported method allows the synthesis of a wide range of five- and six-membered N-alkylated heterocycles in moderate-to-excellent yields starting from predominantly proline and a broad range of benzyl alcohols, and primary and secondary aliphatic alcohols. Examples using pipecolic acid for the construction of piperidine derivatives, as well as the one-pot synthesis of α-amino nitriles, are also shown.

A unique combination of KI/ZnFe2O4 as a catalyst for oxidative Strecker reaction

α-Aminonitriles as key intermediates for the preparation of α-amino acid derivatives, amides, diamines, peptides, proteins and heterocycles were synthesized through methylarene oxidation in the Strecker reaction using a unique combination of KI/ZnFe2O4 as the best catalyst and aqueous tert-butyl hydroperoxide as oxidant. A wide range of amines and methylarenes were converted to the corresponding products. Operational simplicity, short reaction time and recyclability of the catalyst are advantages of this protocol.

Magnetically separable g-C3N4 hybrid nanocomposite: Highly efficient and eco-friendly recyclable catalyst for one-pot synthesis of α-aminonitriles

A magnetically separable graphitic carbon nitride nanocomposite (Fe3O4/g-C3N4) as a catalyst for the three-component condensation reactions of carbonyl compounds, amines and trimethylsilylcyanide was thoroughly investigated. The reaction of these three components was found to be efficient, economical and green and took place in the presence of a catalytic amount of the magnetically separable catalyst to yield the corresponding α-aminonitriles in good to excellent yields. The prepared nanocomposite was characterized using scanning electron microscopy and energy-dispersive X-ray and Fourier transform infrared spectroscopies. The nanocomposite was also found to be reusable could be recovered easily and reused several times without distinct deterioration in its catalytic activity.