FIELD: organic synthesis. SUBSTANCE: method consists in interaction of toluene solution of fullerene(60) with excess of ether solution dibutylmagnesium in presence of zirconacene dichloride as catalyst in quantity 1-3 mol % based on amount of dibutylmagnesium. Reaction is conducted for 12 hr under argon atmosphere and normal conditions at fullerene-to- dibutylmagnesium molar ratio from 1:35 to 1:90. Products can find use organic or organometallic syntheses. EFFECT: extended synthetic possibilities. 1 tbl
Title | Year | Author | Number |
---|---|---|---|
METHOD OF SYNTHESIS OF 1-ARYL(ALKYL)-2-MAGNESIUM HALOGEN(60)- -FULLERENES | 1998 |
|
RU2135506C1 |
METHOD FOR JOINT PREPARATION OF MONO(CYCLOALKYL)DIMAGNESIUMBROMIDEFULLERENES(60) AND BIS(CYCLOALKYL)TETRAMAGNESIUMBROMID- EFULLERENES(60) | 1998 |
|
RU2136688C1 |
METHOD OF SYNTHESIS OF 1-ETHYL-MAGNESIUM HALIDE (60)-FULLERENES | 1998 |
|
RU2135505C1 |
METHOD OF PREPARING 1-(n-PROPYL)-2-MAGNESIUM HALOGEN (60) FULLERENES | 1998 |
|
RU2135504C1 |
METHOD OF PREPARING N-BUTYL SUBSTITUTED C. FULLERENES | 1998 |
|
RU2134255C1 |
METHOD FOR PREPARING 2,3-FULLERENO[60]CYCLOPENTANOLS | 2003 |
|
RU2238262C1 |
METHOD OF SYNTHESIS OF ETHYL-CONTAINING C-FULLERENES | 1998 |
|
RU2133727C1 |
METHOD OF SYNTHESIS OF ETHYLATED FULLERENES | 1997 |
|
RU2119449C1 |
METHOD FOR PRODUCTION OF 1-HYDROXY-2,3-[60]FULLEROCYCLOPENTANECARBOXYLIC ACID ETHYL ESTER | 2005 |
|
RU2283830C1 |
METHOD OF JOINTLY PREPARING 2-ALKYLIDENEMAGNESIUMCYCLOPENTANES AND 2-ALKYL-3-METHYLIDENEMAGNESIUMCYCLOPENTANES | 2003 |
|
RU2245885C1 |
Authors
Dates
1999-09-10—Published
1998-01-12—Filed