93676-72-3Relevant articles and documents
Deplacements homolytiques intramoleculaires. 2. Decomposition du perpentene-4 oate de tert-butyle dans les ethers
Kharrat, A.,Gardrat, C.,Maillard, B.
, p. 2385 - 2390 (2007/10/02)
The thermolysis of tert-butyl perpent-4-enoate 1 in THF led to several compounds; the main product, 5-(2-tetrahydrofuryl)-4-pentanolide (yield 42percent) comes from an induced decomposition of the perester occuring with the addition of 2-tetrahydrofuryl radical to the double bond.A similar reaction was performed at a lower temperature, using butyl perdicarbonate as initiator, but did not define the mechanism (concerted or two-step).The thermolysis of 1 in ethers (THP, oxepane, 1,4-dioxane, dipropyl ether) appears to be a useful synthetic tool: several new γ-lactones have been obtained in this way.