Solvent-free reactions of C60 with active methylene compounds, either with or without carbon tetrabromide, in the presence of bases under high-speed vibration milling conditions

Zhang, TH; Wang, GW; Lu, P; Li, YJ; Peng, RF; Liu, YC; Murata, Y; Komatsu, K

HERO ID

4923643

Reference Type

Journal Article

Year

2004

Language

English

PMID

15188036

HERO ID 4923643
In Press No
Year 2004
Title Solvent-free reactions of C60 with active methylene compounds, either with or without carbon tetrabromide, in the presence of bases under high-speed vibration milling conditions
Authors Zhang, TH; Wang, GW; Lu, P; Li, YJ; Peng, RF; Liu, YC; Murata, Y; Komatsu, K
Journal Organic and Biomolecular Chemistry
Volume 2
Issue 12
Page Numbers 1698-1702
Abstract Solvent-free reactions of C(60) with active methylene compounds, either with or without carbon tetrabromide (CBr(4)), in the presence of a base under high-speed vibration milling (HSVM) conditions were investigated. The reaction of C(60) with diethyl bromomalonate was conducted under HSVM conditions in the presence of piperidine, triethylamine or Na(2)CO(3) to afford cyclopropane derivative. In the presence of CBr(4), methanofullerenes, and could be obtained by the direct reaction of C(60) with diethyl malonate, dimethyl malonate, ethyl acetoacetate and ethyl cyanoacetate, respectively, with the aid of 1,8-diazabicyclo[5,4,0]undec-7-ene, piperidine, triethylamine or Na(2)CO(3). More interestingly, 1,4-bisadducts and were produced by the reaction of C(60) with diethyl malonate and dimethyl malonate in the presence of piperidine, triethylamine or Na(2)CO(3) under HSVM conditions. On the other hand, dihydrofuran-fused C(60) derivatives, and were obtained from the reaction of C(60) with ethyl acetoacetate, 2,4-pentanedione and 5,5-dimethyl-1,3-cyclohexanedione with the aid of a base. Under the same conditions, less activated aryl methyl ketones such as 2-acetylpyridine, 2-acetylpyrazine and acetophenone provided monocarbonylated methanofullerene derivatives, and. Except for the Bingel reactions, all other reactions under the HSVM conditions are considered to proceed according to a single-electron-transfer mechanism.
Doi 10.1039/b403027c
Pmid 15188036
Wosid WOS:000221908100006
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English