3-diethylcarbamoyloxybut-2-enoic acid methyl ester | 1416425-92-7

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 3-diethylcarbamoyloxybut-2-enoic acid methyl ester
• 英文别名: (Z)-methyl-3-((diethylcarbamoyl)oxy)but-2-enoate；methyl 3-(diethylcarbamoyloxy)but-2-enoate；methyl (Z)-3-(diethylcarbamoyloxy)but-2-enoate
• CAS: 1416425-92-7
• 化学式: C₁₀H₁₇NO₄
• 分子量: 215.249
• InChiKey: UHCPGUYZOBEUBU-FPLPWBNLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  55.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  N,N-二乙基甲酰胺 、 乙酰乙酸甲酯 在 叔丁基过氧化氢 、 copper(II) oxide 作用下， 以 水 为溶剂， 反应 4.0h， 生成 3-diethylcarbamoyloxybut-2-enoic acid methyl ester
  参考文献：
  名称：

  通过甲酰胺与1,3-二羰基化合物的氧化偶联，高效超声辅助合成烯醇氨基甲酸酯

  摘要：

  已经报道了通过CuO纳米颗粒作为催化剂和叔丁基氢过氧化物（TBHP）作为氧化剂的甲酰胺与相应的氨基甲酸酯中的1，3-二羰基化合物的声化学氧化偶联。在优化的反应条件下，合成了烯醇氨基甲酸酯的各种衍生物，产率高到高。与常规方法相比，此方法的主要优点是条件温和。

  DOI：

  10.2174/1570178617666191126095420

文献信息

• Synthesis of Carbamates by Direct C-H Bond Activation of Formamides
  作者：Balaji D. Barve、Yang-Chang Wu、Mohamed El-Shazly、Da-Wei Chuang、Yu-Ming Chung、Yi-Hong Tsai、Shou-Fang Wu、Michal Korinek、Ying-Chi Du、Chi-Ting Hsieh、Jeh-Jeng Wang、Fang-Rong Chang

  DOI：10.1002/ejoc.201201160

  日期：2012.12

  catalysed oxidative coupling reaction of formamides with β-keto esters and 2-carbonyl-substituted phenols successfully proceeded through direct C–H bond activation of formamides. The corresponding carbamates were formed with high stereoselectivity under mild reaction conditions. This protocol was successfully applied to the synthesis of three novel halogenated carbamates and a carbaryl insecticide derivative

  铜催化甲酰胺与β-酮酯和2-羰基取代酚的氧化偶联反应通过甲酰胺的直接C-H键活化成功进行。在温和的反应条件下以高立体选择性形成相应的氨基甲酸酯。该协议已成功应用于三种新型卤代氨基甲酸酯和甲萘威杀虫剂衍生物的合成。我们的结果建议使用 6.0 当量。TBHP 对于此类反应至关重要。
• Copper-Catalyzed Oxidative CO Coupling by Direct CH Bond Activation of Formamides: Synthesis of Enol Carbamates and 2-Carbonyl-Substituted Phenol Carbamates
  作者：G. Sathish Kumar、C. Uma Maheswari、R. Arun Kumar、M. Lakshmi Kantam、K. Rajender Reddy

  DOI：10.1002/anie.201105020

  日期：2011.12.2

  Formamide CH bond activation has been achieved under oxidative conditions, using a copper catalyst and tert‐butyl hydroperoxide (TBHP) as the external oxidant (see scheme). This oxidative coupling of a range of dialkyl formamides provides an easy, phosgene‐free route for the selective synthesis of Z‐enol carbamates and 2‐carbonyl‐substituted phenol carbamates in high yields.

  使用铜催化剂和叔丁基氢过氧化物（TBHP）作为外部氧化剂，可以在氧化条件下实现甲酰胺CH键的活化（参见方案）。多种二烷基甲酰胺的这种氧化偶联为高产率地选择性合成Z-烯醇氨基甲酸酯和2-羰基取代的苯甲酸氨基甲酸酯提供了一种简单，无光气的途径。
• Copper nanoparticles on charcoal: an effective nanocatalyst for the synthesis of enol carbamates and amides via an oxidative coupling route
  作者：Dariush Saberi、Sakineh Mansoori、Esmali Ghaderi、Khodabakhsh Niknam

  DOI：10.1016/j.tetlet.2015.11.072

  日期：2016.1

  The catalytic activity of copper nanoparticles on charcoal (Cu/C) was investigated as an environmentally friendly heterogeneous catalyst for the synthesis of enol carbamates and amides via the oxidative coupling of N,N-dialkyl formamides with 1,3-dicarbonyl compounds and aromatic aldehydes with amine hydrochloride salts, respectively. Various enol carbamates and amides were synthesized in moderate to good yields using this method. Moreover, the catalyst could be recovered and subsequently reused in further reactions. (C) 2015 Elsevier Ltd. All rights reserved.