首页> 外国专利> MICROWAVE ASSISTED SYNTHESIS OF 4-TERTBUTYLCALIXNARENES HAVING PHENYL SUBSTITUENTS ON METHYLENE BRIDGES IN PRESENCE OF ALUMINA SUPPORTED KF UNDER SOLVENT FREE CONDITIONS.

MICROWAVE ASSISTED SYNTHESIS OF 4-TERTBUTYLCALIXNARENES HAVING PHENYL SUBSTITUENTS ON METHYLENE BRIDGES IN PRESENCE OF ALUMINA SUPPORTED KF UNDER SOLVENT FREE CONDITIONS.

机译:在无溶剂条件下,铝支撑的KF在微波条件下的微波辅助合成在甲基桥上具有亚苯基取代基的4-叔丁基杯[N]芳烃。

摘要

The present invention relates to a novel process for preparing 2,8,14,20,26,32,38,44- octa phenyl - 5,11,17,23,29,35,41,47- octa-tert butyl 49,50,51,52,53,54,55,56- octahydroxycalix [8]arene (XXXI); 2,8,14,20,26,32-hexa(4-chloro)phenyl-5,l 1,17,23,29, 35 -hexa-tertbuty 1-37,38,39,40,41,42- hexahydroxycalix[6]arene ( XXXII ); 2,8,14,20,26,32-hexa(3-chloro)phenyl-5,11,17,23,29, 35 -hexa- tertbutyl-37,38,39,40,41,42-hexahydroxycalix[6]arene ( XXXIII ); 2,8,14,20,26,32,38,44,50- nona (4- bromo) phenyl-5,11,17,23,29,35,41,47,53- nona-tertbutyl- 55,56,57,58,59,60,61, 62, 63- nonahydroxycalix [9] arene ( XXXIV ); 2,8,14,20,26,32,38,44- octa (4-fluoro) phenyl - 5,11 17,23,29,35,41,47- octa-tertbutyl 49,50,51,52,53,54,55,56- octahydroxycalix [8]arene ( XXXV ); 2,8,14,20,26,32,38,44,50,56-deca (4-nitro) phenyl-5,11,17,23,29,35,41,47,53,59-deca-tertbutyI- 61,62,63,64,65,66,67, 68, 69,70- decahydroxycalix [10] arene ( XXXVI); 2,8,14,20,26,32,38,44,50,56,-deca (3-nitro) phenyl- 5,11,17,23,29,35, 41,47,53,59-deca-tertbutyl- 61,62,63,64,65,66, 67, 68, 69,70-decahydroxycalix [10] arene (XXXVII ); 2,8,14,20,26,32,38,44,50,56,- deca (2-nitro) phenyl-5,11,17,23,29,35,41,47,53,59-deca-tertbutyl- 61,62,63,64,65,66, 67, 68, 69,70- decahydroxycalix [10] arene (XXXVIO ); 2, 8, 14, 20,26,32,38,44,50,56-deca (4-cyano) phenyl-5,11,17,23,29,35,41,47,53,59-deca-tertbutyl-61,62,63,64,65,66,67, 68, 69,70- decahydroxycalix [10] arene (XXXIX); 2,8,14,20,26,32,38,44- octa (4-methoxy) phenyl -5,11„17,23,29,35,41,47- octa-tertbutyl 49,50,51,52,53,54,55,56- octahydroxycalix [8]arene ( XL); 2,8,14,20,26,32,38,44- octa (3-methoxy) phenyl -5,11 „ 17,23,29,35,41,47- octa-tertbutyl 49,50,51,52,53,54,55,56- octahydroxycalix [8]arene (XLI ); 2,8,14,20,26,32-hexa(3,4-dimethoxy)phenyl-5,l 1,17,23,295,-trimethoxy) phenyl - 5,11,17,23 tetra-tertbutyl 25,26,27,28- tetrahydroxycalix [4] arene (XL, 35 -hexa-tertbutyl-37,38,39,40,41,42-hexahydroxyca!ix[6]arene (XLII); 2,8,14,20- tetra (3,4,III); 2,8,14,20- tetra (2,4,6,- trimethoxy) phenyl -5,11,17,23 tetra-tertbutyl 25,26,27,28- tetrahydroxycalix [4] arene (XLIV):- 2,8,14,20- tetra (4-dimethylamino) phenyl - 5,11,17,23 tetra-tertbutyl 25,26,27,28- tetrahydroxycalix [4] arene (XLV) in presence of alumina supported KF under microwave irradiation and solvent free conditions.
机译:本发明涉及制备2,8,14,20,26,32,38,44-辛基苯基-5,11,17,23,29,35,41,47-辛基叔丁基49的新方法,50,51,52,53,54,55,56-八羟基杯[8]芳烃(XXXI); 2,8,14,20,26,32-六(4-氯)苯基-5,1 1,17,23,29,35-六叔丁基1-37,38,39,40,41,42-六羟基杯[6]芳烃(XXXII); 2,8,14,20,26,32-六(3-氯)苯基-5,11,17,23,29,35-六叔丁基-37,38,39,40,41,42-六羟基杯[ 6]芳烃(XXXIII); 2,8,14,20,26,32,38,44,50-壬基(4-溴)苯基-5,11,17,23,29,35,41,47,53-壬基叔丁基-55, 56,57,58,59,60,61,62,63-壬羟基杯[9]芳烃(XXXIV); 2,8,14,20,26,32,38,44-八(4-氟)苯基-5,11 17,23,29,35,41,47-八叔丁基49,50,51,52, 53,54,55,56-八羟基杯[8]芳烃(XXXV); 2,8,14,20,26,32,38,44,50,56-十(4-硝基)苯基-5,11,17,23,29,35,41,47,53,59-十-叔丁基-61,62,63,64,65,66,67,68,69,70-十羟基杯[10]芳烃(XXXVI); 2,8,14,20,26,32,38,44,50,56,-十(3-硝基)苯基-5,11,17,23,29,35,41,47,53,59-十-叔丁基-61,62,63,64,65,66,67,68,69,70-十羟基杯[10]芳烃(XXXVII); 2,8,14,20,26,32,38,44,50,56,-十(2-硝基)苯基-5,11,17,23,29,35,41,47,53,59-十-叔丁基-61,62,63,64,65,66,67,68,69,70-十羟基杯[10]芳烃(XXXVIO); 2,8,14,20,26,32,38,44,50,56-十(4-氰基)苯基-5,11,17,23,29,35,41,47,53,59-十-叔丁基61,62,63,64,65,66,67,68,69,70-十羟基杯[10]芳烃(XXXIX); 2,8,14,20,26,32,38,44-八(4-甲氧基)苯基-5,11„ 17,23,29,35,41,47-八叔丁基49,50,51,52 ,53,54,55,56-八羟基杯[8]芳烃(XL); 2,8,14,20,26,32,38,44-八(3-甲氧基)苯基-5,11-17,23,29,35,41,47-八叔丁基49,50,51,52 ,53,54,55,56-八羟基杯[8]芳烃(XLI); 2,8,14,20,26,32-六(3,4-二甲氧基)苯基-5,1 1,17,23,295,-三甲氧基)苯基-5,11,17,23四叔丁基25,26, 27,28-四羟基杯[4]芳烃(XL,35-六叔丁基-37,38,39,40,41,42-六羟基芳烃[6]芳烃(XLII); 2,8,14,20-四芳烃(3,4,III); 2,8,14,20-四(2,4,6,-三甲氧基)苯基-5,11,17,23四叔丁基25,26,27,28-四羟基杯[4 ]芳烃(XLIV):-2,8,14,20-四(4-二甲基氨基)苯基-5,11,17,23四叔丁基25,26,27,28-四羟基杯[4]芳烃(XLV)在在微波辐射和无溶剂条件下存在氧化铝负载的KF。

著录项

  • 公开/公告号IN2010MU03473A

    专利类型

  • 公开/公告日2013-06-28

    原文格式PDF

  • 申请/专利权人

    申请/专利号IN3473/MUM/2010

  • 申请日2010-12-21

  • 分类号C07C235/32;C07D213/30;

  • 国家 IN

  • 入库时间 2022-08-21 16:41:26

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