2-[(butoxy)methyl]phenol | 13738-64-2

• 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: 2-[(butoxy)methyl]phenol
• 英文别名: 2-Butoxymethyl-phenol；2-(Butoxymethyl)phenol
• CAS: 13738-64-2
• 化学式: C₁₁H₁₆O₂
• 分子量: 180.247
• InChiKey: WANLPVNRLQTCOX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  13
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2,4-二溴-6-丁氧基甲基-苯酚 在 sodium hydroxide 、 镍 作用下， 生成 2-[(butoxy)methyl]phenol
  参考文献：
  名称：

  Chromecek, Chemicke Listy, 1955, vol. 49, p. 1851,1852

  摘要：

  DOI：

文献信息

• Redox-Neutral α-Oxygenation of Amines: Reaction Development and Elucidation of the Mechanism
  作者：Matthew T. Richers、Martin Breugst、Alena Yu. Platonova、Anja Ullrich、Arne Dieckmann、K. N. Houk、Daniel Seidel

  DOI：10.1021/ja501988b

  日期：2014.4.23

  secondary amines and 2-hydroxybenzaldehydes or related ketones react to furnish benzo[e][1,3]oxazine structures in generally good yields. This overall redox-neutral amine α-C–H functionalization features a combined reductive N-alkylation/oxidative α-functionalization and is catalyzed by acetic acid. In contrast to previous reports, no external oxidants or metal catalysts are required. Reactions performed

  环状仲胺和 2-羟基苯甲醛或相关酮反应以通常良好的产率提供苯并[e][1,3]恶嗪结构。这种整体氧化还原中性胺 α-C-H 官能化具有还原 N-烷基化/氧化 α-官能化的组合，并由乙酸催化。与之前的报告相比，不需要外部氧化剂或金属催化剂。在改进的条件下进行的反应导致明显的还原胺化并在涉及氧化第二当量胺的过程中形成邻羟基苄胺。采用密度泛函理论的详细计算研究比较了不同的机械途径，并用于解释观察到的实验结果。此外，
• Zinc-mediated reactions on salicylaldehyde for Botrytis cinerea control
  作者：Antoine Franche、Claire Imbs、Antoine Fayeulle、Franck Merlier、Muriel Billamboz、Estelle Léonard

  DOI：10.1016/j.cclet.2019.08.053

  日期：2020.3

  Chemical control is a necessity and as much as possible, eco-friendly conditions and bioresources to obtain these chemicals should be used. In this context, a series of products was obtained from salicylaldehyde using zinc as a powerful reagent and tested for antifungal activity against Botrytis cinerea

  摘要灰葡萄孢是一种坏死性真菌，会影响各种植物。必须进行化学控制，并应尽可能使用生态友好的条件和生物资源来获得这些化学物质。在这种情况下，使用锌作为强力试剂从水杨醛中获得了一系列产品，并测试了其对灰葡萄孢的抗真菌活性。
• 一种磷酸萘酚喹工艺杂质及其合成方法
  申请人：四川自豪时代药业有限公司

  公开号：CN109503479A

  公开（公告）日：2019-03-22

  本发明公开了一种式(I)所示的未见报道的磷酸萘酚喹工艺杂质的结构，并提供了一种烷基氨甲基苯酚转化为相应的烷基氧甲基苯酚，或者取代的烷基氨甲基苯酚转化为取代的烷基氧甲基苯酚的方法，将烷基氨甲基苯酚或者取代的烷基氨甲基苯酚溶于醇中与二卤代烃和碳酸氢盐反应，利用季铵盐的成环机理和季铵基团良好的离去性制备烷基氧甲基苯酚或取代的烷基氧甲基苯酚。该方法无需使用特殊的反应器，无需对底物中的酚羟基进行保护，操作简单，使用的试剂简单易得，大大缩短了反应步骤，具有较高的应用价值。
• AMINOETHYLATION PROCESS HAVING IMPROVED YIELD OF ARYLOXYALKYLENE AMINE COMPOUNDS AND REDUCED UREA BY-PRODUCTS
  申请人：McDougall Patrick J.

  公开号：US20140073814A1

  公开（公告）日：2014-03-13

  Disclosed is a process for preparing an aryloxyalkylene amine compound via an aminoethylation reaction comprising: a) reacting an aromatic hydroxyl compound in the presence of a basic catalyst with a 2-oxazolidinone compound of the formula II to form an intermediate reaction product; wherein R 3 is selected from the group consisting of hydrogen or lower alkyl having 1 to 6 carbon atoms, R 4 is selected from the group consisting of hydrogen, straight or branched chain alkyl having from one to six carbon atoms, phenyl, alkaryl, or arylalkyl; and b) reacting the intermediate product of step a) with a polyalkylene polyamine.

  揭示了一种通过氨基乙基化反应制备芳基氧基烷胺化合物的过程，包括：a)在碱性催化剂存在下，将芳香羟基化合物与式II的2-噁唑烷酮化合物反应，形成中间反应产物；其中R3选自氢或1至6个碳原子的较低烷基，R4选自氢、一元或分支链烷基（含1至6个碳原子）、苯基、烷基芳基或芳基烷基；b)将步骤a）中间产物与聚烷基聚胺反应。
• N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, And Composition For Transfer And Storage Of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound
  申请人：Shinohata Masaaki

  公开号：US20110133121A1

  公开（公告）日：2011-06-09

  The present invention is a method for producing an N-substituted carbamic acid ester derived from an organic amine from an organic amine, a carbonic acid derivative and a hydroxy composition containing one or more types of hydroxy compounds, wherein the organic amine, the carbonic acid derivative and the hydroxy composition are reacted using a urethane production reaction vessel provided with a condenser, a gas containing the hydroxy composition, the compound having the carbonyl group derived from the carbonic acid derivative, and an ammonia formed as a by-product in the reaction, is introduced into the condenser provided in the urethane production reaction vessel, and the hydroxy composition and the compound having the carbonyl group derived from the carbonic acid derivative are condensed, and wherein a stoichiometric ratio of a hydroxy compound contained in the condensed hydroxy composition to the condensed compound having the carbonyl group derived from the carbonic acid derivative is 1 or more, and a ratio of number of carbonyl groups (—C(═O)—) contained in the compound having the carbonyl group derived from the carbonic acid derivative and number of ammonia molecules contained in the ammonia recovered as a gas from the condenser is 1 or less.

  本发明涉及一种从有机胺、碳酸衍生物和含有一种或多种羟基化合物中制得的N-取代氨基甲酸酯的制备方法，其中使用一种含有冷凝器的脲类生产反应容器反应有机胺、碳酸衍生物和羟基化合物，将含有羟基化合物的气体、来自碳酸衍生物衍生的含有羰基基团的化合物、以及在反应中形成的氨气体引入到脲类生产反应容器中的冷凝器中，使羟基化合物和含有羰基基团的化合物冷凝，其中在冷凝的羟基化合物中所含有的羟基化合物与冷凝的含有羰基基团的化合物中所含有的羰基基团的化合物的比例为1或更多，而且在从冷凝器中回收的氨气体中所含有的羰基基团（—C(═O)—）数与氨分子数的比例为1或更少。