N-cyclohexyl-3-hydroxybutanamide | 91016-74-9

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: N-cyclohexyl-3-hydroxybutanamide
• CAS: 91016-74-9
• 化学式: C₁₀H₁₉NO₂
• 分子量: 185.266
• InChiKey: QATALPFVAFWGDP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  13
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  49.3
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-cyclohexyl-3-hydroxybutanamide 、 溴甲苯 在 sodium hydride 作用下， 以 四氢呋喃 、 mineral oil 为溶剂， 反应 0.5h， 以166 mg的产率得到3-(benzyloxy)-N-cyclohexylbutanamide
  参考文献：
  名称：

  Stereospecific Cross-Coupling of Secondary Alkyl β-Trifluoroboratoamides

  摘要：

  The stereospecific cross-coupling of enantioenriched nonbenzylic secondary alkyl boron compounds has been achieved. The high selectivity toward product formation over an undesired beta-H elimination pathway is achieved via an intramolecular coordination of an ancillary carbonyl to the metal center in the diorganopalladium intermediate.

  DOI：

  10.1021/ja108949w
• 作为产物：
  描述：

  (E)-but-2-enoic acid cyclohexylamide 在 Oxone 、 Cu(MeCN)4*PF6 、 (2R,5R)-1{[(2R,5R)-2,5-diphenylpyrrolidin-1-yl]methylene}2,5-diphenylpyrrolidinium tetrafluoroborate 、 sodium t-butanolate 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 水 为溶剂， 反应 24.0h， 生成 N-cyclohexyl-3-hydroxybutanamide
  参考文献：
  名称：

  对映体富集的仲钾-三氟硼酰胺的合成和 Suzuki-Miyaura 交叉偶联：双硼酸和四（二甲氨基）二硼的催化、不对称共轭加成到 ,-不饱和羰基化合物。

  摘要：

  Enantioenriched 钾β-trifluoroboratoamides 已通过不对称、 铜催化1,4-加成四羟基二硼(BBA) 和四(二甲氨基) 二硼合成α，β-不饱和酰胺。这些二硼试剂使用有效且原子经济的硼源提供了获得所需有机三氟硼酸盐的途径。铜催化的 β-硼酸化扩展到 α,β-不饱和酮和酯。合成的有机三氟硼酸钾的产率高达 92%，对映体比例高达 98:2。当金属转移通过 SE2 机制通过开放过渡态进行时，富含对映体的 β-三氟硼酰胺钾与一系列芳基和杂芳基氯化物成功交叉偶联，具有完全立体化学保真度。

  DOI：

  10.1002/adsc.201300640

文献信息

• An efficient procedure for the synthesis of functionalized 3,4-dihydro-2H-pyrans via catalytic multicomponent reaction
  作者：Alireza Samzadeh-Kermani、Sajjad Ataeifar

  DOI：10.1007/s00706-017-2065-y

  日期：2018.1

  with reactive nitrilium ion derived from the reaction of isocyanides and oxiranes in the presence of lithium salts in PEG-400. The reaction was successfully utilized to synthesize 3,4-dihydro-2H-pyrans in accordance with a simple and environmentally benign procedure. The optimized reaction conditions allowed the selective synthesis of the highly functionalized 3,4-dihydro-2H-pyrans from the commercially

  摘要在该转化中，在PEG-400中存在锂盐的情况下，使丙二腈的共轭碱与衍生自异氰化物和环氧乙烷的反应的反应性氮离子反应。根据简单且环境友好的方法，该反应成功地用于合成3，4-二氢-2 H-吡喃。优化的反应条件允许以可接受的收率从市售起始原料选择性合成高度官能化的3，4-二氢-2 H-吡喃。 图形概要
• Method for preparing optically active beta-butyrolactones
  申请人：Watanabe Shinya

  公开号：US20060046286A1

  公开（公告）日：2006-03-02

  The present invention is to provide a method for preparing easily and efficiently β-butyrolactones and/or optically active 3-hydroxycarboxylic acid derivatives in high optical purity by use of an easily available hydrolase, which are useful as intermediates for pharmaceuticals, agrochemicals and the like. More particularly, the present invention relates to a method for preparing β-butyrolactones and/or optically active 3-hydroxycarboxylic acid derivatives with an optical purity of substantially 100% ee, comprising reacting a β-butyrolactone which is a mixture of optical isomers, with a nucleophilic agent in the presence of a hydrolase, provided that a lipase derived from porcine pancreas is excluded.

  本发明提供了一种使用易得的水解酶高效制备β-丁内酯和/或高光学纯度的光学活性3-羟基羧酸衍生物的方法，这些衍生物作为制药、农药等中间体具有应用价值。更具体地说，本发明涉及一种制备β-丁内酯和/或光学活性3-羟基羧酸衍生物的方法，其光学纯度达到实质上100% ee，包括在水解酶的存在下，用亲核试剂反应混合光学异构体的β-丁内酯，但不包括来自猪胰脂肪酶的酶。
• Copper-Catalyzed β-Boration of α,β-Unsaturated Carbonyl Compounds with Tetrahydroxydiborane
  作者：Gary A. Molander、Silas A. McKee

  DOI：10.1021/ol201900d

  日期：2011.9.2

  The copper-catalyzed beta-boration of alpha,beta-unsaturated carbonyl compounds with tetrahydroxydiborane has been developed. This diboron reagent allows direct, efficient access to boronic acids and their derivatives. Primary, secondary, and tertiary alpha,beta-unsaturated amides are converted to the corresponding beta-trifluoroboratoamides in good to excellent yields. The beta-boration of a variety of alpha,beta-unsaturated esters and ketones is also reported.
• Synthesis and Suzuki-Miyaura Cross-Coupling of Enantioenriched Secondary Potassium β-Trifluoroboratoamides: Catalytic, Asymmetric Conjugate Addition of Bisboronic Acid and Tetrakis(dimethylamino)diboron to α,β-Unsaturated Carbonyl Compounds
  作者：Gary A. Molander、Steven R. Wisniewski、Mona Hosseini-Sarvari

  DOI：10.1002/adsc.201300640

  日期：2013.10.11

  Enantioenriched potassium beta-trifluoroboratoamides have been synthesized via an asymmetric, copper-catalyzed 1,4-addition of tetrahydroxydiboron (BBA) and tetrakis(dimethylamino)diboron to alpha,beta-unsaturated amides. These dibora reagents provide access to the desired organotrifluoroborates using effective and atom economical sources of boron. The copper-catalyzed beta-boration is extended to

  Enantioenriched 钾β-trifluoroboratoamides 已通过不对称、 铜催化1,4-加成四羟基二硼(BBA) 和四(二甲氨基) 二硼合成α，β-不饱和酰胺。这些二硼试剂使用有效且原子经济的硼源提供了获得所需有机三氟硼酸盐的途径。铜催化的 β-硼酸化扩展到 α,β-不饱和酮和酯。合成的有机三氟硼酸钾的产率高达 92%，对映体比例高达 98:2。当金属转移通过 SE2 机制通过开放过渡态进行时，富含对映体的 β-三氟硼酰胺钾与一系列芳基和杂芳基氯化物成功交叉偶联，具有完全立体化学保真度。
• Stereospecific Cross-Coupling of Secondary Alkyl β-Trifluoroboratoamides
  作者：Deidre L. Sandrock、Ludivine Jean-Gérard、Cheng-yi Chen、Spencer D. Dreher、Gary A. Molander

  DOI：10.1021/ja108949w

  日期：2010.12.8

  The stereospecific cross-coupling of enantioenriched nonbenzylic secondary alkyl boron compounds has been achieved. The high selectivity toward product formation over an undesired beta-H elimination pathway is achieved via an intramolecular coordination of an ancillary carbonyl to the metal center in the diorganopalladium intermediate.