1974
DOI: 10.1002/hlca.19740570619
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Arbeiten über Phosphorsäure‐ und Thiophosphorsäureester mit einem heterocyclischen Substituenten. 8. Mitteilung. Das Stäubli‐Verfahren, eine Eintopf‐Kondensation von Thiophosphorverbindungen (, XO,S), Aldehyden und Heterocyclen (mit saurer NH‐Gruppe)

Abstract: The condensation reaction of thiophosphoric compounds 1, aldehydes and heterocycles 3 with an acidic NH‐group in strong mineral acid of specific concentration to asymmetrical compounds 4, called Stäubli procedure, differs from the Mannich‐type reaction catalyzed by weak or dilute acid (aminoalkylation of Hellmann & Opitz) and from the Tscherniac‐Einhorn‐type condensation in concentrated sulfuric acid (amidomethylation of Hellmann). Its main feature is the acidity of the two condensation participants 1 and 3; t… Show more

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Cited by 9 publications
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“…Phosmet was extracted from Imidan [52% Phosmet (w/w), Siegfried Agro, Zofingen, Switzerland) with acetone in a Soxhlet apparatus and, after evaporation under reduced pressure, recrystallized from methanol twice before use. Spectroscopic properties [MS (ESI+), m / z 318 ([M + H] + ); 1 H NMR (DMSO) δ 3.67 (6H, d, CH 3 ), 4.96 (2H, d, CH 2 ), 7.95−7.86 (4H, m, Ar−H); 13 C NMR (DMSO) δ 54.32 (d, CH 3 ), 39.05 (d, CH 2 ), 123.80, 131.55, 135.23 (s, Ar−C), 166.39 (s, CO); IR (ATR) (cm -1 ) 3481, 3025, 2995, 2949, 2867, 1780, 1719, 1612, 1463, 1452, 1406, 1376, 1304, 1279, 1188, 1082, 1072, 914, 831, 819, 797, 722, 692, 676] and melting point of the obtained colorless crystals corresponded to the expected structure and data given in refs (melting point) and 15 (IR spectra). The purity of the recrystallized phosmet was determined by HPLC to be >99% (UV, 220 nm).…”
Section: Methodsmentioning
confidence: 99%
“…Phosmet was extracted from Imidan [52% Phosmet (w/w), Siegfried Agro, Zofingen, Switzerland) with acetone in a Soxhlet apparatus and, after evaporation under reduced pressure, recrystallized from methanol twice before use. Spectroscopic properties [MS (ESI+), m / z 318 ([M + H] + ); 1 H NMR (DMSO) δ 3.67 (6H, d, CH 3 ), 4.96 (2H, d, CH 2 ), 7.95−7.86 (4H, m, Ar−H); 13 C NMR (DMSO) δ 54.32 (d, CH 3 ), 39.05 (d, CH 2 ), 123.80, 131.55, 135.23 (s, Ar−C), 166.39 (s, CO); IR (ATR) (cm -1 ) 3481, 3025, 2995, 2949, 2867, 1780, 1719, 1612, 1463, 1452, 1406, 1376, 1304, 1279, 1188, 1082, 1072, 914, 831, 819, 797, 722, 692, 676] and melting point of the obtained colorless crystals corresponded to the expected structure and data given in refs (melting point) and 15 (IR spectra). The purity of the recrystallized phosmet was determined by HPLC to be >99% (UV, 220 nm).…”
Section: Methodsmentioning
confidence: 99%