2-(1-萘基)-1,3-二恶烷 | 66671-26-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 中文名称: 2-(1-萘基)-1,3-二恶烷
• 英文名称: 2-(naphthalen-1-yl)-1,3-dioxane
• 英文别名: 2-naphthalen-1-yl-1,3-dioxane
• CAS: 66671-26-9
• 化学式: C₁₄H₁₄O₂
• 分子量: 214.264
• InChiKey: MRSKQUQYHTUWQW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  16
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2934999090

反应信息

• 作为产物：
  描述：

  1-萘甲醛 在 povidone-iodine 作用下， 以 乙腈 为溶剂， 反应 6.0h， 生成 2-(1-萘基)-1,3-二恶烷
  参考文献：
  名称：

  可回收PVP-I催化羰基化合物的实用缩醛化和转缩醛化

  摘要：

  已开发出一种新型 PVP-I 催化羰基化合物的缩醛化/转缩醛化，其处理方式温和且易于处理。以羰基化合物或其缩醛为原料成功制备了不同类型的无环和环状缩醛。证明了新开发的催化组合的进一步应用。该方案具有操作简单、反应条件温和、反应时间短、催化剂可回收利用、底物范围广、收率高等特点。

  DOI：

  10.1016/j.tet.2021.132250

文献信息

• METHOD FOR PRODUCING CARBONATE DERIVATIVE
  申请人：NATIONAL UNIVERSITY CORPORATION KOBE UNIVERSITY

  公开号：US20210403409A1

  公开（公告）日：2021-12-30

  The objective of the present invention is to provide a method for producing a polycarbonate safely and efficiently even without using a base. The method for producing a carbonate derivative according to the present invention is characterized in comprising the step of irradiating a high energy light to a composition comprising the halogenated methane and the hydroxy group-containing compound in the presence of oxygen, wherein a molar ratio of a total usage amount of the hydroxy group-containing compound to 1 mole of the halogenated methane is 0.05 or more.

  本发明的目标是提供一种即使不使用碱也能安全高效生产聚碳酸酯的方法。根据本发明的碳酸酯衍生物生产方法的特征在于，在氧气存在的情况下，将含卤代甲烷和含羟基化合物的组合物照射高能光，其中羟基化合物总使用量与1摩尔卤代甲烷的摩尔比为0.05或更高。
• NMR determination of the absolute configuration of chiral 1,2- and 1,3-diols
  作者：Hiroki Fukui、Yukiharu Fukushi、Satoshi Tahara

  DOI：10.1016/s0040-4039(03)00845-1

  日期：2003.5

  1,2- and 1,3-diols examined was derivatized exclusively to a single diastereomeric acetal by the use of a new axially chiral reagent, 2′-methoxy-1,1′-binaphthalene-8-carbaldehyde (MBC). The absolute configuration of the original 1,2- and 1,3-diols was determined by the NOE correlation between the proton signals of the reagent moiety and those of the diol moiety in the acetals.

  通过使用新的轴向手性试剂2'-甲氧基-1,1'-联萘-8-甲醛（MBC），将所检查的每个手性1,2-和1,3-二醇专门衍生为一个非对映体缩醛）。通过缩醛中试剂部分的质子信号和二醇部分的质子信号之间的NOE相关性，确定了原始1,2-和1,3-二醇的绝对构型。
• Rapid Cyclic Acetal and Cyclic Ketal Synthesis Assisted by a Rotary Evaporator
  作者：Fuyao Jiang、Yinzhe Chen、Qian Zhang、Weiding Wang

  DOI：10.1055/a-2293-3243

  日期：2024.11

  Herein, we present a rapid and efficient method for synthesizing cyclic acetals and ketals utilizing a rotary evaporator. Unlike the conventional Dean–Stark dehydration process, which typically demands extended reaction times and copious amounts of organic solvents, our approach affords the synthesis of cyclic acetals and ketals with varying ring sizes in 30 min while using minimal quantities of dimethyl

  在此，我们提出了一种利用旋转蒸发器快速有效地合成环状缩醛和缩酮的方法。与通常需要延长反应时间和大量有机溶剂的传统迪安-斯塔克脱水工艺不同，我们的方法可以在 30 分钟内合成具有不同环尺寸的环状缩醛和缩酮，同时使用最少量的二甲亚砜作为溶剂。该创新方案具有产量高、反应速度快、操作简单、底物适用性广等特点。
• Superacid-Catalyzed Reductive Friedel−Crafts Reaction of Arenes Using Arenecarbaldehyde Acetals
  作者：Shin-ichi Fukuzawa、Teruhisa Tsuchimoto、Tamejiro Hiyama

  DOI：10.1021/jo961897e

  日期：1997.1.1

  Reaction of 2-aryl-1,3-dioxane with arenes in the presence of a catalytic amount of trifluoromethanesulfonic acid gave the corresponding diarylmethanes in good to excellent yields. The acid-catalyzed Friedel-Crafts benzylation of arenes could altenatively be carried out using arenecarbaldehyde and 1,3-propanediol. The reaction was assumed to proceed through a redox process involving hydride shift from the cyclic acetal moiety to the benzylic carbon. The hydride shift was confirmed by the reaction with 5-ethyl-2-phenyl-4,4,6,6-tetradeuterio-1,3-dioxane, wherein more than 90% deuterium was incorporated into the benzylic carbon of the diphenylmethane. Diphenylmethyl ether Ph(2)CHOCH(2)CH(2)CH(2)OH also reacted with benzene to afford diphenylmethane under the same reaction conditions, suggesting that the ether should be the plausible intermediate that underwent the hydride shift.
• JP2006036719A
  申请人：——

  公开号：JP2006036719A

  公开（公告）日：2006-02-09