PERFLUOROHEXANE AS A NOVEL REACTION MEDIUM FOR BROMINATION REACTIONS

被引:20
作者
PEREIRA, SM [1 ]
SAVAGE, GP [1 ]
SIMPSON, GW [1 ]
机构
[1] CSIRO,DIV CHEM & POLYMERS,CLAYTON,VIC 3169,AUSTRALIA
关键词
D O I
10.1080/00397919508012663
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Perfluorohexane is shown to be a good alternative to carbon tetrachloride as a non-toxic, non-ozone-depleting, inert reaction medium for bromination reactions. Yields of brominated products were nearly quantitative and the reaction work-up was easier.
引用
收藏
页码:1023 / 1026
页数:4
相关论文
共 9 条
[1]  
ABBOTT TW, 1943, ORG SYNTH, V2, P270
[2]   FLASH-PHOTOLYSIS OF CHROMIUM HEXACARBONYL IN PERFLUOROCARBON SOLVENTS - OBSERVATION OF A HIGHLY REACTIVE CHROMIUM PENTACARBONYL [J].
BONNEAU, R ;
KELLY, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (03) :1220-1221
[3]   THE ISOMERISATION OF SULPHIDIMINES .3. THE ACTION OF CHLORAMINE-T ON CINNAMYL PHENYL SULPHIDE, AND THE HYDROLYSIS AND OXIDATION OF N-SUBSTITUTED TOLUENE-PARA-SULPHONAMIDES [J].
BRISCOE, PA ;
CHALLENGER, F ;
DUCKWORTH, PS .
JOURNAL OF THE CHEMICAL SOCIETY, 1956, (JUN) :1755-1768
[4]   ELECTROORGANIC CHEMISTRY .2. ELECTROREDUCTION OF VICINAL DIBROMIDES [J].
CASANOVA, J ;
ROGERS, HR .
JOURNAL OF ORGANIC CHEMISTRY, 1974, 39 (16) :2408-2410
[5]  
DYKSTRA HB, 1930, J AM CHEM SOC, V52, P3402
[6]   N-MONOALKYLATION OF SULFONAMIDES [J].
GENSLER, WJ ;
FRANK, FJ ;
DHEER, SK ;
LAUHER, JW .
JOURNAL OF ORGANIC CHEMISTRY, 1971, 36 (26) :4102-&
[7]  
GODD FR, 1923, J CHEM SOC, P3342
[8]  
TSUTSUMI K, 1992, Patent No. 90200349
[9]  
ZHU DW, 1993, SYNTHESIS-STUTTGART, P953