庚烷-2-基苯甲酸酯 | 6624-59-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 庚烷-2-基苯甲酸酯
• 英文名称: heptan-2-yl benzoate
• 英文别名: benzoic acid 1-methylhexyl ester；benzoic acid hept-2-yl ester；2-Heptanol, benzoate
• CAS: 6624-59-5
• 化学式: C₁₄H₂₀O₂
• 分子量: 220.312
• InChiKey: WMGISUKBJZWCDP-UHFFFAOYSA-N

物化性质

• 保留指数：
  1562;1562

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  16
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2916310090

反应信息

• 作为反应物：
  描述：

  庚烷-2-基苯甲酸酯 生成 2-庚醇
  参考文献：
  名称：

  Oxidative decarboxylation of mandelate ethers and α-substituted phenylacetates via dioxetanone generation

  摘要：

  Mandelate ethers are oxidatively decarboxylated via in situ generated dioxetanones using tBuOK and air at ambient temperature leading, after hydrolysis, to the benzoic acid and the corresponding alcohol. The reaction can be extended to alpha-substituted phenylacetates.

  DOI：

  10.1016/s0040-4039(00)79133-7
• 作为产物：
  描述：

  [(heptan-2-yloxy)methyl]benzene 在 air 、 eosin Y-sensitized titanium dioxide 作用下， 以 丙酮 为溶剂， 反应 12.0h， 以76%的产率得到庚烷-2-基苯甲酸酯
  参考文献：
  名称：

  染料敏化半导体的可见光光催化：苄基醚的选择性好氧氧化

  摘要：

  有氧氧化是一种在环境上良性合成精细化学品的有吸引力的方法。另外，染料敏化半导体是用于选择性有机合成的未开发的光催化剂。借助于催化曙红Y敏化的二氧化钛，我们开发了苄基醚有效的好氧光氧化为苯甲酸酯的方法，具有低成本，高原子经济性，广泛的底物范围和用户友好的设置的特点。此外，初步的机理研究表明，反应途径可能需要通过可分离的过氧化物中间体进行光诱导的基于自由基的两步过程。

  DOI：

  10.1021/acscatal.7b03029

文献信息

• Chiral compounds as dopants for liquid crystals
  申请人：MITSUBISHI GAS CHEMICAL COMPANY, INC.

  公开号：EP1380567A1

  公开（公告）日：2004-01-14

  An optically active compound of the general formula (1),    wherein n is an integer of 4 to 8, X is -Ph-COO-Ph-Ph-, -Ph-Ph-COO-Ph-, -Ph-OOC-Ph-Ph-, -Ph-Ph-OOC-Ph-, -Ph-Ph-Ph-, -Cy-COO-Ph-Ph-, -Ph-Ph-OOC-Cy-, -Ph-OOC-Ph-COO-Ph-, -Ph-OOC-Cy-COO-Ph-, -Ph-OOC-Np-COO-Ph-, -Np-OOC-Ph- or -Ph-COO-Np- in which -Ph- is a 1,4-phenylene group, -Cy- is a trans-1,4-cyclohexylene group and -Np- is a 2,6-naphthylene group, and C* is an asymmetric carbon, and a nematic liquid crystal composition containing the above optically active compound. According to the present invention, there is provided a nematic liquid crystal composition containing the optically active compound having a helical twisting power (HTP) of 10 or more and giving a chiral dopant for a nematic liquid crystal, which chiral dopant has a property that the pitch of its induced helix decreases in length with an increase in temperature.

  根据本发明，提供了一种含有上述光学活性化合物的向列型液晶组合物。所述光学活性化合物具有10或以上的螺旋扭曲力(HTP)，并为向列型液晶提供手性掺杂剂，该手性掺杂剂具有其诱导螺旋的螺距随温度升高而缩短的性质。
• Brønsted Acid Mediated Nucleophilic Functionalization of Amides through Stable Amide C−N Bond Cleavage; One‐Step Synthesis of 2‐Substituted Benzothiazoles
  作者：Srabani Maity、Arnab Roy、Surajit Duari、Subrata Biswas、Asma M. Elsharif、Srijit Biswas

  DOI：10.1002/ejoc.202100645

  日期：2021.7.7

  A TFA mediated general and simple synthetic protocol to directly cleave stable amide C−N bonds by a variety of alcohol and amine nucleophiles has been developed. Natural alcohols such as menthol and cholesterol took part in the reaction under the present reaction conditions to generate the desired esters. Structurally important 2-substituted benzothiazole derivatives have been synthesized in one pot

  已经开发了一种 TFA 介导的通用和简单合成方案，可通过各种醇和胺亲核试剂直接裂解稳定的酰胺 CN 键。天然醇如薄荷醇和胆固醇在本反应条件下参与反应生成所需的酯。使用 2-氨基苯硫酚作为亲核试剂，在一锅中合成了结构上重要的 2-取代苯并噻唑衍生物。
• Catalytic conversion of ketones to esters <i>via</i> C(O)–C bond cleavage under transition-metal free conditions
  作者：Murugan Subaramanian、Palmurukan M. Ramar、Jagannath Rana、Virendra Kumar Gupta、Ekambaram Balaraman

  DOI：10.1039/d0cc03312j

  日期：——

  The catalytic conversion of ketones to esters via C(O)–C bond cleavage under transition-metal free conditions is reported. This catalytic process proceeds under solvent-free conditions and offers an easy operational procedure, broad substrate scope with excellent selectivity, and reaction scalability.

  据报道，在无过渡金属条件下，酮通过C（O）-C键的裂解催化转化为酯。该催化过程在无溶剂条件下进行，并提供了简便的操作步骤，宽泛的底物范围和出色的选择性以及反应可扩展性。
• ANOMALOUS ORIENTATIONAL EFFECTS DURING BENZOYLOXYLATIONS BY “SILVER BROMIDE DIBENZOATE”
  作者：Derek Bryce-Smith、Neil S. Isaacs、Seddeg O. Tumi

  DOI：10.1246/cl.1984.1471

  日期：1984.9.5

  formed from bromine and silver benzoate reacts with both arenes and alkanes to form aryl and alkyl benzoates, respectively. Highly unusual substituent effects are observed in the benzoyloxylations of arenes. Electron-withdrawing groups (e.g. –NO2, –CN, –CO–) on the aromatic ring facilitate reaction though directing the attacking reagent exclusively to the meta position. In alkanes, tertiary positions are

  由溴和苯甲酸银形成的固体络合物分别与芳烃和烷烃反应形成芳基苯甲酸酯和烷基苯甲酸酯。在芳烃的苯甲酰氧基化中观察到非常不寻常的取代基效应。芳环上的吸电子基团（例如–NO2、–CN、–CO–）通过将攻击试剂专门导向间位来促进反应。在烷烃中，三级位置最容易受到攻击。
• Iron Perchlorate on Silica Gel as Multi-purpose Reagent for Catalysis of Closure and Rupture of Carbon-Oxygen Bond in Epoxides, Alcohols, and Esters
  作者：P. Salechi、M. M. Khodaei、S. B. Ghareghani、A. R. Motlagh

  DOI：10.1023/b:rujo.0000003154.92028.84

  日期：2003.6

  Aliphatic alcohols and water in the presence of catalytic amounts of Fe3+ ion introduced as iron(Ill) perchlorate on silica gel carrier perform efficient regiospecific opening of an epoxy ring. Carbon acids esterification with various type alcohols was carried out using the system Fe(ClO4)(3)-silica gel in dichloromethane under conditions excluding solvolysis. Acetylation and formylation of alcohols was performed by efficient transesterification with ethyl acetate and ethyl formate.