期刊文献+
任意字段
题名或关键词
题名
关键词
文摘
作者
第一作者
机构
刊名
分类号
参考文献
作者简介
基金资助
栏目信息

异戊烯醛合成路线及其工业化研发的评述 被引量：1

PROGRESS FOR PREPARATION OF PRENAL AND COMMENT OF ITS INDUSTRIALIZATION RESEARCH
下载PDF
导出
摘要 介绍了以3-甲基-3-丁烯-1-醇、3-甲基-2-丁烯-1-醇,2-甲基-3-丁炔-2-醇为起始原料的异戊烯醛合成路线。结合各个国家的工业化程度,详细评价了异戊烯醛各种合成工艺的优缺点,并提出了异戊烯醛工业化研发的发展趋势。 Prenal is a kind of important intermediate for synthesis of drugs,spices and pesticides.The methods which mainly employed 3-methyl-3-buten-1-ol,3-methyl-2-buten-1-ol or 2-methyl-3-butyn2-ol as starting materials for preparation of prenal were summarized.Based on the degree of industrialization in some countries,advantages and disadvantages of their process for preparation of prenal were summarized and commented in detail.Development trend of process which used for producing prenal was proposed.
作者 吕耀宏 吕星鑫
机构地区 浙江理工大学
出处 《精细石油化工》 CAS CSCD 北大核心 2014年第1期73-78,共6页 Speciality Petrochemicals
关键词 异戊烯醛 3-甲基-2-丁烯-1-醛 柠檬醛 合成 工业化 prenal 3-methyl-2-buten-1-al preparation citral industrialization
分类号 TQ224.1 [化学工程—有机化工]
  • 相关文献

参考文献43

  • 1Seeber G, Grossschmidt D, M/urer T, et al. Precious metal catalysts with low metal loading {or oxidative dehy drogenations: US, 20120277476AlePh. 2012-11-01.
  • 2Badisehe Anilin I Soda Fabrik AG. Improvements in the partial hydrogenation of acetylene compounds: GB, 871804A[P]. 1961-06-28.
  • 3Murer T, Seeber G, Abdallah R,et al. Use of a suppor- ted catalyst containing precious metal for oxidative dehy- drogenation: US,2011015446Al[P]. 2011-01-20.
  • 4钱洪胜,董金锋,吕叔敏,商志才.柠檬醛及中间体的合成[J].应用化学,2012,29(3):270-274. 被引量：3
  • 5Meissner B, Fliege W, Woerz O, et aI. Preparation of 3-methyl- 2-buten- 1-al : US, 4192820[P]. 1980-03-11.
  • 6Hindley N C, Andrews D A. A process for the manufacture of oxo compounds: GB, 1457025[P]. 1974-04-26.
  • 7梁鑫淼,王心亮,刘仁华,等.一种催化空气氧化醇制备醛或酮的方法:CN,101486621B[P].2009-07-22.
  • 8Winslow E V. Conversion of acetylenic alcohols in thevapor phase: US, 2524866[P]. 1950-10-10.
  • 9Brenner K, Ruppel W, Woerz O, et al. Tube bundle reactor, use thereof in exothermic organic reactions, and preparation of ketones and aldehydes Using same: US,5149884[P]. 1992-09-22.
  • 10Hindley N C, Andrews D A. Process for the manufacture of oxo compounds: GB, 1409323[P3. 1972 -11- 02.

二级参考文献19

  • 1李若华.高纯柠檬醛生产条件选择[J].广西化工,1993,22(3):11-14. 被引量：3
  • 2余申义.异戊烯酸制备方法的改进[J].化学试剂,1994,16(5):320-320. 被引量：2
  • 3石晓华,周舞阗,陈新志.2,2-二甲基环丙烷甲酸的合成与拆分[J].高校化学工程学报,2005,19(3):384-387. 被引量：16
  • 4Toru SATO,Manabu SENO,Teruzo ASAHARA.Telomerization of Isobutylene with Carbon Tetrachloride and Synthesis of ββ-Dimethylacrylic Acid from Its 1:1 Adduct (1,1,1,3-Tetrachloro-3-methylbutane)[J].Journal of Synthetic Organic Chemistry,Japan,1974,32(3),184-187.
  • 5Bernd Meissner Heidelberg,Werner Fliege Otterstadt,Otto Woerz Ludwigshafen.,et al.Preparation of 3-methyl-2-buten-1-al[P].US4192820,1980.
  • 6Pierre Chabardes.Ti/Cu and Ti/Ag catalysts for the isomerisation of α-acetylenic alcohols into α,β-ethylenic carbonyl derivatives[J].Tetrahedron Letters.1988,29(48):6253-6256.
  • 7Saucy G, Marbet R, Lindlar H, et al. Uber eine neue Synthese yon Citral und Verwandten Verbindungen [ J ]. Helv Chim Acta, 1959,42 (6) : 1945-1955.
  • 8Hosogai T, Nishida T, Itoi K. Manufacture of Unsaturated Carbonyl Compounds :JP 51048608 [ P ], 1974-10-18.
  • 9Pauling H, Andrews D A, Hindley N C. The Rearrangement of α-Acetylenic Alcohols to α,β-Unsaturated Carbonyl Compounds by Silylvanadate Catalysts[ J]. Helv Chim Acta,1976,59(4):1233-1243.
  • 10Pierre C. Ti/Cu and Ti/Ag Catalysts for the Isomerisation of α-Acetylenic Alcohols into α,β-Ethylenic Carbonyl Derivatives [ J ]. Tetrahedron Lett, 1988,29 (48) :6253-6256.

共引文献2

引证文献1

精细石油化工
2014年 第1期

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