| Abstract: | Treatment of 2,2,4,4‐tetramethylcyclobutane‐1,3‐dione ( 6 ) in THF with CF3SiMe3 in the presence of tetrabutylammonium fluoride (TBAF) yielded the corresponding 3‐(trifluoromethyl)‐3‐(trimethylsilyl)oxy]cyclobutanone 7 (Scheme 1) via nucleophilic addition of a CF anion at the C?O group and subsequent silylation of the alcoholate. Under similar conditions, the ‘monothione' 1 reacted to give thietane derivative 8 (Scheme 2), whereas in the case of ‘dithione' 2 only the dispirodithietane 9 , the dimer of 2 , was formed (Scheme 3). A conceivable mechanism for the formation of 8 is the ring opening of the primarily formed CF3 adduct A followed by ring closure via the S‐atom (Scheme 2). In the case of thiobenzophenones 4 , complex mixtures of products were obtained including diarylmethyl trifluoromethyl sulfide 10 and 1,1‐diaryl‐2,2‐difluoroethene 11 (Scheme 4). Obviously, competing thiophilic and carbophilic addition of the CF anion took place. The reaction with 9H‐fluorene‐9‐thione ( 5 ) yielded only 9,9′‐bifluorenylidene ( 14 ; Scheme 6); this product was also formed when 5 was treated with TBAF alone. Treatment of 4a with TBAF in THF gave dibenzhydryl disulfide ( 15 ; Scheme 7), whereas, under similar conditions, 1 yielded the 3‐oxopentanedithioate 17 (Scheme 9). The reaction of dithione 2 with TBAF led to the isomeric dithiolactone 16 (Scheme 8), and 3 was transformed into 1,2,4‐trithiolane 18 (Scheme 10). |
