Kinetic and mechanistic study on the thermal reactivity of stabilized phosphorus ylides, part 3: [(Acetyl)(arylcarbamoyl)methylene]triphenylphosphoranes and [(alkoxycarbonyl)(arylcarbamoyl)methylene]triphenylphosphoranes and their thiocarbamoyl analogues

✍ Scribed by R. Alan Aitken; Nouria A. Al-Awadi; Graham Dawson; Osman El-Dusouqui; Kamini Kaul; Ajith Kumar

• Book ID: 102447208
• Publisher: John Wiley and Sons
• Year: 2006
• Tongue: English
• Weight: 219 KB
• Volume: 39
• Category: Article
• ISSN: 0538-8066
• DOI: 10.1002/kin.20208

✦ Synopsis

Abstract

A series of five [(acetyl)(arylcarbabmoyl)methylene]triphenyl‐phosphoranes 1a–e and their thiocarbamoyl analogues 2a–e, [(alkoxycarbonyl)(arylcarbamoyl)methylene]triphenylphosphoranes 3a–e and their thiocarbamoyl analogues 4a–e were prepared and fully characterized. All ylides are found under conditions of flash vacuum pyrolysis to fragment giving arylisocyanate or isothiocyanate and acetyl ylides or alkoxy ylides which undergo thermal extrusion of Ph~3~PO. A kinetic study shows that these reactions are unimolecular and are of first‐order nature with no significant substituent effect. The thiocarbamoyl ylides 2 react from 4.6 to 42 times faster than their carbamoyl ylides 1, while the thiocarbamoyl ylides 4 react from 6.6 to 20.9 times faster than their carbamoyl ylides 3. © 2006 Wiley Periodicals, Inc. Int J Chem Kinet 39: 6–16, 2007