期刊文献+

合成工艺条件对对叔丁氧基甲苯收率的影响

Effects of synthetic process conditions on the yield of p-tert-butoxy-methylbenzene
下载PDF
导出
摘要 为克服现有对叔丁氧基甲苯合成方法的缺点,以对甲苯酚和异丁烯为原料,在相转移剂和硫酸水溶液催化剂存在下,研究了反应温度、催化剂用量等合成工艺条件对对叔丁氧基甲苯收率的影响。结果表明,在m(对甲苯酚)/m(硫酸)/m(四丁基溴化铵)为100.0∶3.0∶0.9,n(异丁烯)/n(对甲苯酚)为1.6,反应温度为20℃,反应时间为5 h的优选合成工艺条件下,对叔丁氧基甲苯收率大于78%。 In order to overcome the shortcomings of the existing synthesis method of p -tert - butoxy- methylbenzene, the effects of synthetic process conditions, such as reaction temperature, cat- alyst level, on the yield of p -tert -butoxy -methyl- benzene were investigated with p - cresol and isobutene as raw materials in the presence of phase transfer agent and sulfuric acid solution catalyst. The results showed that under the optimized conditions of reaction time 5 h, m (p - cresol)/m ( sulfuric acid) / m (tetrabutylammonium bromide) 100.0 : 3.0 : 0. 9, n (isobutene)/rt ( p - cresol ) 1.6, reaction temper- ature 20℃ , the yield of p - tert - butoxy - methyl- benzene was over 78%.
出处 《石化技术与应用》 CAS 2015年第1期22-25,共4页 Petrochemical Technology & Application
关键词 对叔丁氧基甲苯 对甲苯酚 异丁烯 相转移剂 O-烷基化反应 p - tert - butoxy - methylbenzene p - cresol isobutene phase transfer agent O - alkylation
  • 相关文献

参考文献14

  • 1梁希,张金钟,陈安齐.内酸酐去对称化方法合成多羟基环己基β-氨基酸手性中间体[J].厦门大学学报(自然科学版),2006,45(6):792-796. 被引量:3
  • 2Chi Y G, Samuel H G. , William C P, et al. Concise/32 - amino acid synthesis via organo catalyic aminomethyllation:US,7820858 B2[P].2010-10-26.
  • 3Chi Y G, Emily P, William C, et al. Practical synthesis of enantio- merically pure/32 - amino acid via proline - catalyzed diastereose- lective aminomethylation of aldehydes [ J ]. J Am Chem Soc, 2007,129(18) :6050 -6055.
  • 4Keegstra M A,Peters T H A,Brandsma L. Copper(I) Halide cat- alysed synthesis of alkyl aryl and alkyl heteroaryl ethers[ J]. Tet- rahedron, 1992,48 ( 17 ) :3 633 - 3 652.
  • 5Naidu A B,Jaseer E A, Sekar G. General, mild, and intermolecu- lar Ullmann - type synthesis of diaryl and alkyl aryl ethers cata- lyzed by diol - copper (l) complex [ J ]. J Orq Chem, 2009,74 (10) :3 675 -3 679.
  • 6Naidu A B,Sekar G. An efficient intermolecular Binam - copper (I) catalyzed Ullmznntype coupling of aryl iodides/bromides with aliphatic alcohols[ J]. Tetra - h - Edon,2008 ,49 :3 147 - 3 151.
  • 7陈杨英,赵德丰.Cu(I)卤化物催化合成烷基芳基醚的研究[J].化学工程师,2001,15(1):5-6. 被引量:2
  • 8Camps F, Coil J, Moreto J M. Improved procedure for preparation of t - alkyl aryl ethers [ J ]. Communications Synthesis, 1982 (3) :186 -188.
  • 9Eric E D,Feixia C,Kim S I. Cesium promoted 0 - alkylation of alcohols for the efficient ether synthesis [ J]. Tetrahedron Let- ters,1999(40) :1 843 -1 846.
  • 10Fuhrmann E,Talbiersky J. Synthesis of alkyl aryl ethers by cata- lytic williamson ether synthesis with weak alkylation agents[ J]. Orgnic Process Research & Deyelopment,2005 (9) :206 - 21 1.

二级参考文献10

  • 1Kunisch F,Babczinski P,Arlt D,et al.Pharmaceuticals containing substituted cyclohex-2-ene derivatives and their use in combatting diseases:Germany,De 4028046 A1[P].1992.
  • 2Mittendorf J,Buchholz J B,Fey P,et al.Efficient asymmetric synthesis of β-amino acids BAY 10-8888/PLD-118,a novel antifungal for the treatment of yeast infections[J].Synthesis,2003,1:136.
  • 3Appella D h,LePlae P,Raguse T L,et al.(R,R,R)-2,5-Diaminocyclohexanecarboxylic acid,a building block for water-soluble,helix-forming β-peptides[J].J.Org.Chem.,2000,65:4766.
  • 4Wipf P,Wang X.Diels-Alder approaches to ring-functionalized cyclic β-amino acids[J].Tetrahedron Lett.,2000,41:8747.
  • 5Perrin D D,Armarego W L F.Purification of Laboratory Chemicals[M].3rd ed.Oxford:Pergamon Press,1988.
  • 6Masesane I B,Steel P G.Stereoselective routes to polyhydroxylated cyclohexyl-β-amino Acids[J].Synlett,2003,5:735.
  • 7Kobayashi S,Kamiyama K,Iimori T,et al.Creation of novel chiral synthons with enzymes and applications to natural product Synthesis[J].Tetrahedron Lett.,1984,25:2557.
  • 8Bolm C,Schiffers I,Dinter C L,et al.Practical and highly enantioselective ring opening of cyclic meso-anhydrides mediated by cinchona alkaloids[J].J.Org.Chem.,2000,65:6984.
  • 9Bernardi A,Arosio D,Dellavecchia D,et al.Improved synthesis of both enantiomers of trans-cyclohex-4-ene-1,2-dicarboxylic acid[J].Tetrahedron Asymmetry,1999,10:3403.
  • 10Kobayashi S,Kamiyama K,Ohno M.The first enantioselective synthesis of fortamine,the 1,4-diaminocyclitol moiety of fortimicin A,by chemicoenzymatic approach[J].J.Org.Chem.,1990,55:1169

共引文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部