121668-40-4Relevant academic research and scientific papers
RING OPENING OF 2,2,4,6,6-PENTACHLORO-4-FENYLDIMEDONE AFFORDING AN α,α-DICHLORO-γ-BUTYROLACTONE
Buyck, L. De,Pooter, H. De,Schamp, N.
, p. 793 - 794 (2007/10/02)
An α,α-Dichloro-γ-butyrolactone 4 was formed after ring opening of 2,2,4,6,6-pentachloro-4-fenyldimedone with NaOAc-HOAc in aqueous dioxane.The ring opening in methanol gave a δ-ketoester 5 which was cyclised with Na2CO3 to afford the cyclic enol ether 6.
