2,2-二甲基-1,3-二噁烷-4-甲醇 | 56476-33-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 2,2-二甲基-1,3-二噁烷-4-甲醇
• 英文名称: (2,2-dimethyl-[1,3]dioxan-4-yl)-methanol
• 英文别名: 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane；(2,2-Dimethyl-1,3-dioxan-4-yl)methanol
• CAS: 56476-33-6
• 化学式: C₇H₁₄O₃
• 分子量: 146.186
• InChiKey: VHFPDSDOOGPPBS-UHFFFAOYSA-N

物化性质

• 沸点：
  207.7±15.0 °C(Predicted)
• 密度：
  1.004±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  38.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2,2-二甲基-1,3-二噁烷-4-甲醇 、 2-chloro-3-cyclohexylnaphthalene-1,4-dione 以94%的产率得到
  参考文献：
  名称：

  HUDSON, A. T.;PETHER, M. J.;FERRIGE, A. G.;LINDON, J. C., J. CHEM. SOC. PERKIN TRANS., 1982, N 8, 1933-1936

  摘要：

  DOI：
• 作为产物：
  描述：

  丙酮 、 1,2,4-丁三醇 在 对甲苯磺酸 作用下， 生成 2,2-二甲基-1,3-二噁烷-4-甲醇 、 2,2-dimethyl-4-(2-hydroxyethyl)-1,3-dioxolane
  参考文献：
  名称：

  A Further Synthesis of an Analogue of the Antifungal/Antiherbivore Lipid from Avocado

  摘要：

  牛油果二烯（1a）的饱和外消旋衍生物（1b）的进一步合成 二烯 (1a) 的饱和外消旋衍生物 (1b) ((R,Z,Z)-2-hydroxy-4-oxohenicosa-12,15-dien-1-yl 醋酸酯；"persin"）。

  DOI：

  10.1071/c98063

文献信息

• [EN] N-PHENYLPYRAZOLE DERIVATIVES AS PESTICIDES<br/>[FR] DERIVES DE N-PHENYLPYRAZOLE EN TANT QUE PESTICIDES
  申请人：BAYER CROPSCIENCE SA

  公开号：WO2006000314A1

  公开（公告）日：2006-01-05

  The invention relates to polar 5-aminopyrazole carbamate derivatives of formula (I) or salts thereof: (I), wherein the various symbols are as defined in the description, to processes for their preparation, to compositions thereof, and to their use for the control of pests (including arthropods and helminths).

  该发明涉及极性5-氨基吡唑碳酰胺衍生物的公式(I)或其盐： (I)，其中各种符号如描述中定义，涉及它们的制备过程，包含它们的组合物，以及它们用于控制害虫（包括节肢动物和蠕虫）的使用。
• PRODUCTION OF CYCLIC ACETALS OR KETALS USING SOLID ACID CATALYSTS
  申请人：Terrill Daniel Latham

  公开号：US20120330032A1

  公开（公告）日：2012-12-27

  A process for making a cyclic compounds such as cyclic acetal or cyclic ketones by feeding aldehyde or ketone compounds and polyhydroxyl compounds to a reaction zone at a molar ratio of polyhydroxyl compounds to aldehyde or ketone compounds of at least 3:1, reacting these compounds in the presence of a solid acid such as an acidic ion exchange resin, to generate a liquid reaction mixture without separating water from the reaction mixture as it is being formed in the reaction mixture, withdrawing the liquid reaction mixture from the reaction zone as a liquid product stream, and feeding the liquid reaction product stream to a distillation column to separate cyclic acetal compounds from unreacted polyhydroxyl compounds, and optionally recycling back the unreacted polyhydroxyl compounds to the reaction zone. The process produces cyclic acetal compounds in yields of at least 90% with long catalyst life. The process is also suitable to make cyclic ketals from ketone compounds.

  通过将醛或酮化合物和多羟基化合物以多羟基化合物与醛或酮化合物的摩尔比至少为3:1的比例送入反应区域，在固体酸的存在下（如酸性离子交换树脂）中反应这些化合物，生成液体反应混合物而不将水从反应混合物中分离出来，将液体反应混合物从反应区域中作为液体产品流撤出，并将液体反应产物流送入蒸馏塔以从未反应的多羟基化合物中分离出环状缩醛化合物，并可选择性地将未反应的多羟基化合物回收到反应区域。该过程以至少90%的产率生产环状缩醛化合物，并具有长寿命的催化剂。该过程也适用于从酮化合物制备环状缩酮。
• PRODUCTION OF CYCLIC ACETALS OR KETALS USING LIQUID-PHASE ACID CATALYSTS
  申请人：Terrill Daniel Latham

  公开号：US20120330033A1

  公开（公告）日：2012-12-27

  A process for making a cyclic compounds such as cyclic acetal or cyclic ketones by feeding aldehyde or ketone compounds and polyhydroxyl compounds to a reaction vessel at a molar ratio of polyhydroxyl compounds to aldehyde or ketone compounds of at least 3:1, reacting these compounds in the presence of a homogeneous acid catalyst to generate a liquid phase homogeneous reaction mixture containing the acid catalyst without separating water from the reaction mixture as it is being formed in the reaction mixture, withdrawing the liquid phase homogeneous reaction mixture from the reaction vessel as a liquid product stream, and feeding the liquid reaction product stream to a distillation column to separate cyclic acetal compounds from unreacted polyhydroxyl compounds, and optionally recycling back the unreacted polyhydroxyl compounds and/or acid catalyst to the reaction vessel. The process produces cyclic acetal compounds in high yields. The process is also suitable to make cyclic ketals from ketone compounds.

  通过将醛或酮化合物和多羟基化合物以多羟基化合物与醛或酮化合物的摩尔比至少为3:1的比例加入到反应容器中，通过在均相酸催化剂存在下反应这些化合物，生成含有酸催化剂的液相均相反应混合物，而不从反应混合物中分离水，将液相均相反应混合物从反应容器中作为液体产品流撤出，并将液体反应产物流送入蒸馏塔以将环状缩醛化合物与未反应的多羟基化合物分离，并可选择性地将未反应的多羟基化合物和/或酸催化剂回收到反应容器中。该过程以高产率生产环状缩醛化合物。该过程也适用于从酮化合物制备环状缩酮。
• Preparation of isopropylidene acetals from butane-1,2,4-triol and its cyclopropane congeners
  作者：Konstantin N. Prokhorevich、Andrei V. Bekish

  DOI：10.1016/j.tetlet.2010.05.126

  日期：2010.8

  Features of isopropylidene acetal synthesis from butane-1,2,4-triol and its cyclopropane congeners were studied. Procedures for the preparation and purification of the respective acetonides have been developed.

  研究了由1,2,4-丁三醇及其环丙烷同源物合成异亚丙基缩醛的特性。已经开发了制备和纯化各个丙酮化物的方法。
• Dihydropyridine derivatives
  申请人：AJINOMOTO CO. INC

  公开号：US20020147222A1

  公开（公告）日：2002-10-10

  Compounds having a selective N-type calcium channel antagonistic activity are provided. Dihydropyridine derivatives represented by the following formula: 1 analogs thereof and pharmaceutically acceptable salts thereof have an activity of selectively inhibiting the action of N-type calcium channel, and they are used as therapeutic agents for various diseases relating to N-type calcium channel.

  提供具有选择性N型钙通道拮抗活性的化合物。以下式表示的二氢吡啶衍生物：1的类似物及其药用盐具有选择性抑制N型钙通道作用的活性，它们可用作与N型钙通道相关的各种疾病的治疗剂。