3,4-Dimethyl-benzoesaeure-N,N-diethylamid | 15930-58-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3,4-Dimethyl-benzoesaeure-N,N-diethylamid
• 英文别名: Uuwstohuwmzqct-uhfffaoysa-；N,N-diethyl-3,4-dimethylbenzamide
• CAS: 15930-58-2
• 化学式: C₁₃H₁₉NO
• mdl: MFCD01215987
• 分子量: 205.3
• InChiKey: UUWSTOHUWMZQCT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.461
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  3,4-二甲基苯甲酸 在 氯化亚砜 、 三乙胺 作用下， 生成 3,4-Dimethyl-benzoesaeure-N,N-diethylamid
  参考文献：
  名称：

  通过无金属催化的活化烯烃分子内氰基氰化反应不对称合成含季碳中心的功能化二氢萘醌

  摘要：

  通过路易斯碱催化的不对称烯丙基烷基化反应以及随之而来的前所未有的烯烃不对称分子内酰基氰化反应，开发了一种新型的无金属催化环化反应。该方案为制备对映体富集的稠密官能化二氢萘醌以及对映体纯的带有季碳中心的3,3-二取代的邻苯二酚提供了独特而便捷的途径。

  DOI：

  10.1021/ol501427h

文献信息

• HMF and furfural: Promising platform molecules in rhodium-catalyzed carbonylation reactions for the synthesis of furfuryl esters and tertiary amides
  作者：Xinxin Qi、Rong Zhou、Han-Jun Ai、Xiao-Feng Wu

  DOI：10.1016/j.jcat.2019.11.008

  日期：2020.1

  esters and tertiary amides has been developed. 5-Hydroxymethylfurfural (HMF) was used as both substrate and CO surrogate for the first time in a carbonylation reaction, and both alkyl and aryl iodides were tolerated well to afford the desired furfuryl esters in moderate to good yields. In addition, furfural was also utilized as a CO source for the synthesis of tertiary amides. A variety of tertiary amides

  已经开发了涉及铑催化的糠基酯和叔酰胺的羰基合成的生物质。在羰基化反应中，首次使用5-羟甲基糠醛（HMF）作为底物和CO替代物，烷基碘和芳基碘均耐受良好，以中等至良好的收率提供了所需的糠酸酯。另外，糠醛也用作合成叔酰胺的一氧化碳来源。以中等至优异的产率获得了具有良好官能团相容性的多种叔酰胺。值得注意的是，在不存在其他氧化剂的情况下，叔胺通过C N键裂解途径用作胺源。
• NITROGEN CONTAINING HETEROARYL COMPOUNDS
  申请人：Bleicher Konrad

  公开号：US20110306589A1

  公开（公告）日：2011-12-15

  The invention is concerned with novel nitrogen-containing heteroaryl compounds of formula (I) wherein A 1 , A 2 , R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are as defined in the description and in the claims, as well as physiologically acceptable salts and esters thereof. These compounds inhibit PDE10A and can be used as therapeutics.

  这项发明涉及一种新颖的含氮杂环芳基化合物，其化学式为（I），其中A1、A2、R1、R2、R3、R4、R5和R6如描述和索赔中所定义，并且其生理上可接受的盐和酯。这些化合物抑制PDE10A并可用作治疗药物。
• PROCESS FOR PRODUCING ALPHA, ALPHA- DIFLUOROAMINE
  申请人：National University Corporation Hokkaido University

  公开号：EP1813596A1

  公开（公告）日：2007-08-01

  A process for producing an α,α-difluoroamine which comprises using hydrogen fluoride and a Lewis base in specific amounts in the halogen-fluorine exchange reaction using an α,α-dihaloamine as the substrate. The process can be industrially applied, enables to obtain the object compound in a short time at a great yield and can be conducted easily with excellent productivity.

  一种生产α,α-二氟化胺的工艺，包括在以α,α-二卤胺为底物的卤-氟交换反应中使用一定量的氟化氢和路易斯碱。该工艺可应用于工业，能在短时间内以高产率获得目标化合物，而且操作简便，生产效率极高。
• REPELLENT COMPOSITIONS FOR INSECTS AND OTHER ARTHROPODS
  申请人：International Centre of Insect and Physiology and Ecology

  公开号：EP3030076A2

  公开（公告）日：2016-06-15
• PROCESS FOR PRODUCING ALPHA, ALPHA-DIFLUOROAMINE
  申请人：Fukuhara Tsuyoshi

  公开号：US20090177012A1

  公开（公告）日：2009-07-09

  A process for producing an α,α-difluoroamine which comprises using hydrogen fluoride and a Lewis base in specific amounts in the halogen-fluorine exchange reaction using an α,α-dihaloamine as the substrate. The process can be industrially applied, enables to obtain the object compound in a short time at a great yield and can be conducted easily with excellent productivity.