1-(3-phenylpropyl)-1-pentyl ether

• 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: 1-(3-phenylpropyl)-1-pentyl ether
• 英文别名: 1-(pentyloxy)-3-phenylpropane；pentyl-(3-phenyl-propyl)-ether；Pentyl-(3-phenyl-propyl)-aether；3-Pentoxypropylbenzene
• 化学式: C₁₄H₂₂O
• 分子量: 206.328
• InChiKey: FRGWOWNNHHPCIG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  15
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  pentyloxy-acetonitrile 在 氢氧化钾 、 乙醚 、 一水合肼 、 三乙二醇 作用下， 反应 2.0h， 生成 1-(3-phenylpropyl)-1-pentyl ether
  参考文献：
  名称：

  The Kishner Reduction-Elimination. II. α-Substituted Pinacolones^1,2

  摘要：

  DOI：

  10.1021/ja01617a036

文献信息

• Improved Procedure for the Reductive Acetylation of Acyclic Esters and a New Synthesis of Ethers
  作者：David J. Kopecky、Scott D. Rychnovsky

  DOI：10.1021/jo9914521

  日期：2000.1.1

  acetylation procedure allows a wide variety of esters to be converted into the corresponding alpha-acetoxy ethers in good to excellent yields. It was found that, under mild acidic conditions, many alpha-acetoxy ethers can be further reduced to the corresponding ethers. This net two-step ester deoxygenation is an attractive alternative to the classical Williamson synthesis for certain ethers.

  描述了用于无环酯和二酯的DIBALH还原乙酰化的优化方案。该还原性乙酰化方法可以将多种酯以良好或优异的产率转化为相应的α-乙酰氧基醚。发现在弱酸性条件下，许多α-乙酰氧基醚可以进一步还原成相应的醚。对于某些醚，这种净的两步酯脱氧是经典威廉姆森合成的一种有吸引力的替代方法。
• An Efficient and Convenient Method for the Direct Conversion of Alkyl Silyl Ethers into the Corresponding Alkyl Ethers Catalyzed by Iron(III) Chloride
  作者：Takeshi Oriyama、Katsuyuki Iwanami、Kentaro Yano

  DOI：10.1055/s-2005-872120

  日期：——

  Various alcohol silyl ethers were readily and efficiently transformed into the corresponding alkyl ethers in high yields by the use of aldehydes combined with triethylsilane in the presence of a catalytic amount of iron(III) chloride.

  在催化量的氯化铁 (III) 存在下，通过使用醛与三乙基硅烷结合，各种醇甲硅烷基醚容易且高效地转化为相应的烷基醚，产率很高。
• Iron(III) Chloride-catalyzed Reductive Etherification of Carbonyl Compounds with Alcohols
  作者：Katsuyuki Iwanami、Kentaro Yano、Takeshi Oriyama

  DOI：10.1246/cl.2007.38

  日期：2007.1

  A facile reductive etherification of carbonyl compounds can be performed by the reaction with alcohols and triethylsilane catalyzed by iron(III) chloride. The corresponding alkyl ethers are obtaine...

  羰基化合物的简单还原醚化可以通过在氯化铁 (III) 的催化下与醇和三乙基硅烷反应来进行。得到相应的烷基醚...
• [EN] PROCESS FOR THE PRODUCTION OF 4-SUBSTITUTED CHROMANES VIA GOLD CATALYSIS<br/>[FR] PROCÉDÉ DE PRODUCTION DE CHROMANES 4-SUBSTITUÉS CATALYSÉ PAR L'OR
  申请人：COUNCIL SCIENT IND RES

  公开号：WO2013088455A1

  公开（公告）日：2013-06-20

  Disclosed herein is single step process for the synthesis of 4-aryl substituted chromanes of compound of formula 2 comprising subjecting 3-aryloxy-l-phenylpropan-l-ol of formula 1 to gold (III) chloride-catalyzed intramolecular Friedel-Crafts reaction to obtain 4-aryl substituted chromanes. The invention further discloses novel 4-substituted Chromane compounds.

  本文公开了一种合成式为2的4-芳基取代色烷的单步过程，包括将式为1的3-芳氧基-1-苯基丙醇经过金（III）氯化物催化的分子内Friedel-Crafts反应，制得4-芳基取代色烷。本发明还公开了新型的4-取代色烷化合物。
• Derivatives of 4-(2-amino -1-hydroxyethyl)phenol as agonists of the Beta2 adrenergic receptor
  申请人：Duran Carlos Puig

  公开号：US20090042933A1

  公开（公告）日：2009-02-12

  A compound of formula (I) or a pharmaceutically-acceptable salt, solvate or stereoisomer thereof wherein R 1 is a group chosen from —CH 2 OH and —NHC(O)H; R 2 is a hydrogen atom or R 1 together with R 2 form the group —NH—C(O)—CH═CH—, wherein the nitrogen atom is bound to the carbon atom in the phenyl ring holding R 1 and the carbon atom is bound to the carbon atom in the phenyl ring holding R 2 ; R 3 is chosen from a hydrogen atom, a halogen atom and groups chosen from —SO—R 5 , —SO 2 —R 5 , —NH—CO—NH 2 , —CO—NH 2 , hydantoino, C 1-4 alkyl, C 1-4 alkoxy and —SO 2 NR 5 R 6 ; R 4 is chosen from a hydrogen atom, a halogen atom and a C 1-4 alkyl group; R 5 is chosen from a C 1-4 alkyl group and a C 3-8 cycloalkyl group; R 6 is independently chosen from a hydrogen atom and a C 1-4 alkyl group; n, p and q are independently 0, 1, 2, 3 or 4; m and s are independently 0, 1, 2 or 3; and r is 0, 1 or 2 with the provisos that at least one of m and r is not 0, the sum n+m+p+q+r+s is 7, 8, 9, 10, 11, 12 or 13, and the sum q+r+s is 2, 3, 4, 5 or 6.

  化合物的化学式（I）或其药学上可接受的盐、溶剂化合物或立体异构体，其中R1是从—CH2OH和—NHC（O）H中选择的基团；R2是氢原子或R1与R2一起形成—NH—C（O）—CH═CH—的基团，其中氮原子与持有R1的苯环中的碳原子结合，碳原子与持有R2的苯环中的碳原子结合；R3从氢原子、卤原子和从—SO—R5、—SO2—R5、—NH—CO—NH2、—CO—NH2、hydantoino、C1-4烷基、C1-4烷氧基和—SO2NR5R6中选择的基团；R4从氢原子、卤原子和C1-4烷基中选择；R5从C1-4烷基和C3-8环烷基中选择；R6独立选择从氢原子和C1-4烷基中选择；n、p和q独立选择0、1、2、3或4；m和s独立选择0、1、2或3；r为0、1或2，但至少有一个m和r不为0，n+m+p+q+r+s之和为7、8、9、10、11、12或13，且q+r+s之和为2、3、4、5或6。