1-phenoxy-3-(propylamino)propan-2-ol | 39631-74-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 1-phenoxy-3-(propylamino)propan-2-ol
• 英文别名: 1-phenoxy-3-propylamino-propan-2-ol；1-Phenoxy-3-(propylamino)-2-propanol
• CAS: 39631-74-8
• 化学式: C₁₂H₁₉NO₂
• mdl: MFCD11213269
• 分子量: 209.288
• InChiKey: JPDURUUZCYERAP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  15
• 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：
  41.5
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  苯酚 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 、 丙酮 为溶剂， 反应 48.0h， 生成 1-phenoxy-3-(propylamino)propan-2-ol
  参考文献：
  名称：

  伯胺在溶剂指导下的环氧开环反应，用于合成β-氨基醇

  摘要：

  摘要 据报道，在没有任何催化剂的情况下，可以由多种环氧化物和伯直链伯胺高效合成β-氨基醇，从而具有高收率和区域选择性。多种极性混合溶剂体系允许仲氨基醇相对于叔氨基醇的选择性形成。反应范围扩展到各种带有复杂官能团的芳族和脂族取代的环氧化物和伯胺。 据报道，在没有任何催化剂的情况下，可以由多种环氧化物和伯直链伯胺高效合成β-氨基醇，从而具有高收率和区域选择性。多种极性混合溶剂体系允许仲氨基醇相对于叔氨基醇的选择性形成。反应范围扩展到各种带有复杂官能团的芳族和脂族取代的环氧化物和伯胺。

  DOI：

  10.1055/s-0036-1588356

文献信息

• Benzimidazole derivatives and their use as a medicament
  申请人：Poitout Lydie

  公开号：US20090170922A1

  公开（公告）日：2009-07-02

  A subject of the present application is new benzimidazole derivatives of formula in which A, Y, R 1 , R 2 , R 3 and R 4 represent different variable groups. These products have an antagonist activity of GnRH (Gonadotropin-Releasing Hormone). The invention also relates to pharmaceutical compositions containing said products and their use for the preparation of a medicament.

  本申请的主题是公式中A、Y、R1、R2、R3和R4代表不同变量基团的新苯并咪唑衍生物。这些产物具有GnRH（促性腺激素释放激素）的拮抗活性。本发明还涉及含有所述产物的制药组合物及其用于制备药物的用途。
• Solvent-free aminolysis of aliphatic and aryloxy epoxides with sulfated zirconia as solid acid catalyst
  作者：Arpan K. Shah、Manish Kumar、Sayed H.R. Abdi、Rukhsana I. Kureshy、Noor-ul H. Khan、Hari C. Bajaj

  DOI：10.1016/j.apcata.2014.08.024

  日期：2014.9

  Single-step and two-steps synthetic procedure for the synthesis of sulfated zirconia (SZ) was developed, which were calcined at 500, 600 and 700 degrees C and characterized by various physico-chemical methods such as PXRD, FTIR, surface area, microanalysis, NH3-TPD and DRIFT analysis. These SZ materials were then employed as solid acid catalysts for the aminolysis of different aliphatic/aromatic terminal, aryloxy and meso epoxides with aromatic and aliphatic amines under ambient conditions. Amongst the catalyst prepared, SZ-2-600 prepared in two-steps and 600 degrees C calcined was found to be the most efficient catalyst to give beta-amino alcohols in up to 98% yield and >99% regioselectivity. The SZ catalyst was successfully recycled and reused up to six catalytic runs with intact efficiency. (C) 2014 Elsevier B.V. All rights reserved.
• Fe(OH)3 nano solid material: An efficient catalyst for regioselective ring opening of aryloxy epoxide with amines under solvent free condition
  作者：Arpan K. Shah、K. Jeya Prathap、Manish Kumar、Sayed H.R. Abdi、Rukhsana I. Kureshy、Noor-ul H. Khan、Hari C. Bajaj

  DOI：10.1016/j.apcata.2013.10.003

  日期：2014.1

  Iron hydroxide-Fe(OH)(3) and iron oxides (Fe3O4 and Fe2O3) were successfully prepared and characterized. These materials were employed as efficient and environmentally benign heterogeneous catalysts for the epoxide ring opening reaction of various alyloxy, terminal and meso epoxides with aromatic and aliphatic amines under solvent free condition at room temperature. Out of these, nano-sized Fe(OH)(3) (IH-1) showed better catalytic activity to give the product beta-amino alcohols in excellent yield (up to similar to 96%) and high regioselectivity in 10-360 min. The catalyst was successfully recycled and reused eight times with no loss in catalytic activity. (C) 2013 Published by Elsevier B.V.
• Petrow et al., Journal of Pharmacy and Pharmacology, 1956, vol. 8, p. 666,667, 670
  作者：Petrow et al.

  DOI：——

  日期：——
• Sorokin; Wenkowa, 1957, # 25, p. 58,61, 67
  作者：Sorokin、Wenkowa

  DOI：——

  日期：——