The technique is applied to conversions that proceed via unimolecular pathways. 2-Acetoxydioxane, when heated at 425 °C converts to the highly reactive dioxene, via loss of acetic acid. 3 2-Furonitrile has been prepared by flash-dehydration of 2-furoic acid amide or oxime over molecular sieves.4 The strained ring benzocyclobutenone has been prepared by FVP from a simple benzoyl chloride precursor.5
McNab, Hamish "Chemistry without reagents: synthetic applications of flash vacuum pyrolysis" Aldrichimica Acta 2004, volume 37, pp. 19–26. http://www.sigmaaldrich.com/ifb/acta/v37/acta-vol37-2004.html#20 http://www.sigmaaldrich.com/ifb/acta/v37/acta-vol37-2004.html#20 ↩
Wentrup, Curt "Flash (Vacuum) Pyrolysis Apparatus and Methods" Australian Journal of Chemistry 2014, volume 67, 1150–1165. doi:10.1071/CH14096 /wiki/Doi_(identifier) ↩
Matthew M. Kreilein, James C. Eppich, Leo A. Paquette "1,4-Dioxene" Org. Synth. 2005, volume 82, pp. 99. doi:10.15227/orgsyn.082.0099 /wiki/Doi_(identifier) ↩
Jacqueline A. Campbell; McDougald, Graham; McNab, Hamish; Rees, Lovat; Tyas, Richard (2007). "Laboratory-scale synthesis of nitriles by catalyzed dehydration of amides and oximes under flash vacuum pyrolysis (FVP) conditions". Synthesis. 2007 (20): 3179–3184. doi:10.1055/s-2007-990782. /wiki/Doi_(identifier) ↩
Peter Schiess; Ppatibha V. Barve; Franz E. Dussy; Andreas Pfiffner (1995). "Benzocyclobutenone By Flash Vacuum Pyrolysis". Org. Synth. 72: 116. doi:10.15227/orgsyn.072.0116. /wiki/Doi_(identifier) ↩