Dimethyl carbonate for environmentally benign reactions

被引:148
作者
Ono, Y
机构
[1] Department of Chemical Engineering, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo
关键词
D O I
10.1351/pac199668020367
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dimethyl carbonate (DMC) is a unique molecule having a versatile reactivity, The transesterification of DMC with phenol gives methyl phenyl carbonate, which is converted into diphenyl carbonate (DPC) by the disproportionation. MoO3/SiO2 is an active catalyst for both reactions. DPC is an essential monomer in the non-phosgene route for polycarbonates. The methoxycarbonylation of aniline gives methyl N-phenyl carbamate in the presence of a lead compound. This reaction offers a non-phosgene route to isocyanates. As a methylating agent, DMC can be a substitute for methyl halides and dimethyl sulfate, toxic and corrosive chemicals. Phenylacetylene, aniline and phenol are selectively methylated with DMC over zeolites in the vapor-phase. The reaction of DMC with silica offers a simple and clean method for synthesizing Si(OCH3)(4).
引用
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页码:367 / 375
页数:9
相关论文
共 46 条
[1]   DIRECT SYNTHESIS OF TETRAMETHOXYSILANE FROM RICE HULL ASH BY REACTION WITH DIMETHYL CARBONATE [J].
AKIYAMA, M ;
SUZUKI, E ;
ONO, Y .
INORGANICA CHIMICA ACTA, 1993, 207 (02) :259-261
[2]   AN EXCEPTIONALLY MILD, CATALYTIC HOMOGENEOUS METHOD FOR THE CONVERSION OF AMINES INTO CARBAMATE ESTERS [J].
ALPER, H ;
HARTSTOCK, FW .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1985, (16) :1141-1142
[3]   CONVERSION OF PRIMARY AMINES TO CARBAMATE ESTERS USING PALLADIUM-CHLORIDE AND DI-TERT-BUTYL PEROXIDE - DOUBLE CARBONYLATION OF SECONDARY-AMINES [J].
ALPER, H ;
VASAPOLLO, G ;
HARTSTOCK, FW ;
MLEKUZ, M ;
SMITH, DJH ;
MORRIS, GE .
ORGANOMETALLICS, 1987, 6 (11) :2391-2393
[4]  
AWATO I, 1993, SCIENCE, V259, P1538
[5]   THE "BIS(SALICYLALDEHYDE)ETHYLENEDIIMINE COBALT(II)-CATALYZED OXIDATIVE CARBONYLATION OF PRIMARY AND SECONDARY-AMINES [J].
BENEDINI, F ;
NALI, M ;
RINDONE, B ;
TOLLARI, S ;
CENINI, S ;
LAMONICA, G ;
PORTA, F .
JOURNAL OF MOLECULAR CATALYSIS, 1986, 34 (02) :155-161
[6]   SELECTIVE RUTHENIUM CARBONYL CATALYZED REDUCTIVE CARBONYLATION OF AROMATIC NITRO-COMPOUNDS TO CARBAMATES [J].
CENINI, S ;
PIZZOTTI, M ;
CROTTI, C ;
PORTA, F ;
LAMONICA, G .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1984, (19) :1286-1287
[7]  
CENTI S, 1988, J ORG CHEM, V53, P1243
[8]  
CUSUMANO JA, 1992, CHEMTECH, P482
[9]  
FROST JW, 1995, CHEM BRIT, V3, P207
[10]  
Fu Z., UNPUB