(ethoxymethyl)dipropylamine | 67232-13-7

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: (ethoxymethyl)dipropylamine
• 英文别名: N-(ethoxymethyl)-N-propylpropan-1-amine
• CAS: 67232-13-7
• 化学式: C₉H₂₁NO
• 分子量: 159.272
• InChiKey: KZGFTKAJCVXVJI-UHFFFAOYSA-N

物化性质

• 沸点：
  183.1±13.0 °C(Predicted)
• 密度：
  0.835±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  11
• 可旋转键数：
  7
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  12.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (ethoxymethyl)dipropylamine 在 甲基三氯硅烷 作用下， 以 乙腈 为溶剂， 反应 0.08h， 以90%的产率得到N,N-dipropylmethaniminium chloride
  参考文献：
  名称：

  A New Convenient Synthesis of Dialkyl(methylene)ammonium Chloride

  摘要：

  提出了一种新的、简便的合成方法或二烷基（亚甲基）氯化铵，其原料是宝石氨基醚和甲基三氯硅烷（一种甲基氯硅烷工业合成的副产品）。

  DOI：

  10.1055/s-1986-31627
• 作为产物：
  描述：

  聚合甲醛 、 乙醇 、 二正丙胺 在 potassium carbonate 作用下， 生成 (ethoxymethyl)dipropylamine
  参考文献：
  名称：

  A New Convenient Synthesis of Dialkyl(methylene)ammonium Chloride

  摘要：

  提出了一种新的、简便的合成方法或二烷基（亚甲基）氯化铵，其原料是宝石氨基醚和甲基三氯硅烷（一种甲基氯硅烷工业合成的副产品）。

  DOI：

  10.1055/s-1986-31627

文献信息

• Synthesis of new functionalized aminomethylphosphonites and their derivatives
  作者：Andrey A. Prishchenko、Mikhail V. Livantsov、Olga P. Novikova、Ludmila I. Livantsova、Valery S. Petrosyan

  DOI：10.1002/hc.20620

  日期：——

  aminomethylation of the several esters of hypophosphorous acid using chloro-, alkoxy-, and amino-substituted methylamines of various structure is proposed as convenient method for the synthesis of new functionalized aminomethylphosphonites and bis(aminomethyl)phosphinates. Also O,O-diethyl(pivaloyl)phosphonite is successfully applied in the aminomethylation as a synthetic analog of unstable diethoxyphosphine.

  提出了使用各种结构的氯代、烷氧基和氨基取代的甲胺对几种次磷酸酯进行氨基甲基化，作为合成新型功能化氨基甲基亚膦酸酯和双（氨基甲基）次膦酸酯的简便方法。O,O-二乙基（新戊酰基）亚膦酸酯也作为不稳定二乙氧基膦的合成类似物成功地应用于氨甲基化。© 2010 Wiley Periodicals, Inc. 杂原子化学 21:361–367, 2010; 在 wileyonlinelibrary.com 上在线查看这篇文章。DOI 10.1002/hc.20620
• Method for producing high-purity quaternary ammonium salt
  申请人：Nishida Tetsuo

  公开号：US20100044617A1

  公开（公告）日：2010-02-25

  A process for preparing a high-purity quaternary ammonium salt comprising: (1) adding an oxide or hydroxide of a Group 1, 2, 12 or 13 metal to a quaternary ammonium salt containing a protonic acid salt of a tertiary amine as an impurity and thereby neutralizing the tertiary amine protonic acid salt with the metal oxide or hydroxide to convert the acid salt to a tertiary amine and water and to convert the metal oxide or hydroxide to a metal salt at the same time, and (2) removing the tertiary amine, water and metal salt produced from the system.

  一种制备高纯度季铵盐的方法，包括以下步骤：(1)向含有三级胺质子酸盐杂质的季铵盐中加入1、2、12或13族金属的氧化物或氢氧化物，通过金属氧化物或氢氧化物中和三级胺质子酸盐，将酸盐转化为三级胺和水，并同时将金属氧化物或氢氧化物转化为金属盐；(2)从体系中去除产生的三级胺、水和金属盐。
• PROCESS FOR PRODUCTION OF HIGHLY PURE QUATERNARY AMMONIUM SALT
  申请人：Otsuka Chemical Co., Ltd.

  公开号：EP2098518A1

  公开（公告）日：2009-09-09

  A process for preparing a highly pure quaternary ammonium salt comprising: (1) adding a quaternary ammonium hydroxide salt or quaternary ammonium carbonate to a quaternary ammonium salt containing a protonic acid salt of a tertiary amine as an impurity and thereby neutralizing the tertiary amine protonic acid salt with the quaternary ammonium hydroxide salt or carbonate to convert the acid salt to a tertiary amine and water and to convert the quaternary ammonium hydroxide salt or carbonate to a quaternary ammonium salt at the same time, and (2) removing the tertiary amine and water produced from the system.

  一种制备高纯季铵盐的工艺，包括 (1) 将氢氧化季铵盐或碳酸季铵盐加入到含有叔胺质子酸盐作为杂质的季铵盐中，从而用氢氧化季铵盐或碳酸季铵盐中和叔胺质子酸盐，将酸盐转化为叔胺和水，并同时将氢氧化季铵盐或碳酸季铵盐转化为季铵盐，以及 (2) 从系统中清除产生的叔胺和水。
• Reaction of triphenyl(phenylethynyl)phosphonium bromide with α-aminoethers, dipiperidinomethane, and secondary amines
  作者：G. B. Bagdasaryan、P. S. Pogosyan、G. A. Panosyan、M. G. Indzhikyan

  DOI：10.1134/s1070363207050088

  日期：2007.5

  The reactions of triphenyl(phenylethynyl)phosphonium bromide with (alpha-aminoethers lead to formation of triphenyl(2-amino-2-phenylvinyl)phosphonium bromides. In the case of acyclic aminoethers, this reaction is accompanied by the formation of the corresponding amine hydrobromide and triphenylphosphine oxide by a scheme analogous to that of alkaline hydrolysis of phosphonium salts and involving attack of the amine on the phosphorus atom. The reaction of the same salt with diethyl- or dipropylamine affords hydrobromides of the latter, while with piperidine, together with salts, its adduct by the triple bond is formed. Piperidinomethane with the same salt forms triphenylphosphonium (2-phenyl-2-piperidinovinyl)phosphonium bromide.
• Prishchenko, A.A.; Livantsov, M.V.; Petrosyan, V.S., Russian Journal of General Chemistry, 1994, vol. 64, # 8.2, p. 1181 - 1193
  作者：Prishchenko, A.A.、Livantsov, M.V.、Petrosyan, V.S.

  DOI：——

  日期：——