neopentyl 4-methoxybenzoate | 3581-72-4

• 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: neopentyl 4-methoxybenzoate
• 英文别名: Neopentyl-4-methoxybenzoat；p-Anisic acid, neopentyl ester；2,2-dimethylpropyl 4-methoxybenzoate
• CAS: 3581-72-4
• 化学式: C₁₃H₁₈O₃
• 分子量: 222.284
• InChiKey: LJNIFDFCWAKMHD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  16
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  新戊醇 、 大茴香酸 在 硫酸 作用下， 以 甲苯 为溶剂， 以100%的产率得到neopentyl 4-methoxybenzoate
  参考文献：
  名称：

  Caron, Stephane; Hawkins, Joel M., Journal of Organic Chemistry, 1998, vol. 63, # 7, p. 2053 - 2055

  摘要：

  DOI：

文献信息

• Synthesis of Unsymmetrical <i>N</i>-Heterocyclic Carbene–Nitrogen–Phosphine Chelated Ruthenium(II) Complexes and Their Reactivity in Acceptorless Dehydrogenative Coupling of Alcohols to Esters
  作者：Xiaochun He、Yaqiu Li、Haiyan Fu、Xueli Zheng、Hua Chen、Ruixiang Li、Xiaojun Yu

  DOI：10.1021/acs.organomet.9b00071

  日期：2019.4.22

  dehydrogenative coupling of alcohols to esters, and the excellent isolated yields of esters were given in a catalyst loading of 1% for para- and meta-substituted benzyl alcohols and long-chain primary alcohols. Although some ortho-substituted benzyl alcohols displayed a relatively low reactivity due to the steric hindrance and the coordination of electron donor with the ruthenium center, the good product

  两种新型的钌络合物期RuH（CO）氯（PPH 3）（κ 2 -CP）（1）和[ FAC -RuH（CO）（PPH 3）（κ 3 -CNP）]氯（2）轴承不对称ñ -杂环合成了卡宾-氮-膦（CNP）并通过1 H NMR，31 P NMR和HRMS进行了表征。配合物2的结构通过单晶X射线衍射进一步确认。阴离子交换实验证明复合物2可以转化为复合物1在解决方案中。两种络合物在醇与酯的无受体脱氢偶联中显示出高催化性能，并且在对-和间-取代的苄醇和长链伯醇的催化剂负载量为1％时，酯的分离产率极佳。尽管由于空间位阻以及电子给体与钌中心的配位，一些邻位取代的苄醇显示出较低的反应性，但延长反应时间仍可获得良好的产物收率。特别地，该系统成功地实现了两种不同伯醇之间的酯的脱氢交叉偶联。
• Acceptorless Dehydrogenative Cross-Coupling of Primary Alcohols Catalyzed by an N-Heterocyclic Carbene–Nitrogen–Phosphine Chelated Ruthenium(II) Complex
  作者：Ling Zhao、Xiaochun He、Tianhua Cui、Xufeng Nie、Jiaqi Xu、Xueli Zheng、Weidong Jiang、Maolin Yuan、Hua Chen、Haiyan Fu、Ruixiang Li

  DOI：10.1021/acs.joc.1c02828

  日期：2022.4.1

  The acceptorless dehydrogenative cross-coupling of primary alcohols to form cross-esters with the liberation of H2 gas was enabled using a [RuCl(η6-C6H6)(κ2-CNP)][PF6]Cl complex as the catalyst. This sustainable protocol is applicable to a broad range of primary alcohols, particularly for the sterically demanding ones, featuring good functional group tolerance and high selectivity. The good catalytic

  使用 [RuCl(η 6 -C 6 H 6 )(κ 2 -CNP)][PF 6 ]Cl 络合物，可以实现伯醇的无受体脱氢交叉偶联以形成交叉酯并释放 H 2气体催化剂。这种可持续的协议适用于广泛的伯醇，特别是对于空间要求高的伯醇，具有良好的官能团耐受性和高选择性。良好的催化性能可归因于氮-膦功能化的N-杂环卡宾（CNP）配体，它采用面配位模式以及配位苯的容易解离。
• The effect of<i>para</i>-substitution on the mass spectra of arylsulphonate esters of neopentanol
  作者：Orval A. Mamer、Abeysinghe A. Padmapriya、George Just

  DOI：10.1002/oms.1210201210

  日期：1985.12

  AbstractThe mass spectra of several para‐substituted benzenesulfonic and benzoic esters of unlabelled and 1,1‐d2‐neopentyl alcohol are examined and compared. Evidence is presented of migration of the aryl group from the sulfur to an oxygen atom in the molecular ions of the sulfonic esters. The nature of the fragmentation processes and the occurrence of metastable ions for these processes are both much more dependent upon the polarity of the para substituent in the case of the sulfonates than for the benzoates. Elimination of C5H10 occurs from the molecular ion of the p‐methoxysulfonate with transfer to the residual ion of a hydrogen atom selected randomly from the alkyl fragment, while in the case of the p‐aminosulfonate, incomplete randomization is demonstrated.
• Caron, Stephane; Hawkins, Joel M., Journal of Organic Chemistry, 1998, vol. 63, # 7, p. 2053 - 2055
  作者：Caron, Stephane、Hawkins, Joel M.

  DOI：——

  日期：——