A new one pot method for the conversion of aldehydes into nitriles using hydroxyamine and phthalic anhydride

Tetrahedron Letters

Volumn 39, Issue 23, 1998, Pages 4047-4050

  Wang, Eng Chi ^a   Lin, Gow Juin ^a  

^a KAOHSIUNG MEDICAL UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ACID ANHYDRIDE; ALDEHYDE; AMINE; NITRILE; PHTHALIC ACID DERIVATIVE;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION; REACTION ANALYSIS; TECHNIQUE;

EID: 0032482529     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00654-6     Document Type: Article

References (38)

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36. 2O, it gave oxime (0.56 g, 77 %) with the recovery of aldehyde (0.29 g); in entry f, it gave oxime (0.35 g, 52 %) with the recovery of aldehyde (0.58 g).
37. 2O in entry j, it gave 4-acetoxybenzoxime (0.09 g, 11 %) and gave oxime (0.53 g, 86 %) with the recovery of aldehyde (0.06 g).
38. 2O in entry 1, it gave N-Acetylpyrrole-2-carbonitrile (0.15 g, 33 %); and gave oxime (0.18 g, 58 %) with the recovery of aldehyde (0.15 g).