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(1R,2R,4S)-2-(6-bromopyridine-2-yl)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol | 256428-16-7

中文名称
——
中文别名
——
英文名称
(1R,2R,4S)-2-(6-bromopyridine-2-yl)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
英文别名
(1R,2R,4S)-2-(6-bromopyridin-2-yl)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
(1R,2R,4S)-2-(6-bromopyridine-2-yl)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol化学式
CAS
256428-16-7
化学式
C15H20BrNO
mdl
——
分子量
310.234
InChiKey
DYFZCMYLDMHXJM-VQISRLSMSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.8
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    33.1
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (1R,2R,4S)-2-(6-bromopyridine-2-yl)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol三苯基膦 、 nickel dichloride 、 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 以47%的产率得到(1R,2R,4S)-2-[6-[6-[(1R,2R,4S)-2-hydroxy-1,3,3-trimethyl-2-bicyclo[2.2.1]heptanyl]pyridin-2-yl]pyridin-2-yl]-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
    参考文献:
    名称:
    New chiral 2,2′-bipyridine diols as catalysts for enantioselective addition of diethylzinc to benzaldehyde
    摘要:
    New C-2-symmetric chiral 2,2'-bipyridine diols were prepared from readily available homochiral materials such as menthone and camphor. Their catalytic activities in the reaction of diethylzinc with benzaldehyde to give 1-phenyl-1-propanol were studied. In all cases, the yields were good and enantioselectivities up to 95% were observed. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0957-4166(99)00399-7
  • 作为产物:
    描述:
    2,6-二溴吡啶(1R)-1,3,3-三甲基二环[2.2.1]庚-2-酮正丁基锂 作用下, 以 四氢呋喃正己烷 为溶剂, 以98%的产率得到(1R,2R,4S)-2-(6-bromopyridine-2-yl)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
    参考文献:
    名称:
    Butyllithium-Mediated Coupling of Aryl Bromides with Ketones under In-Situ-Quench (ISQ) Conditions: An Efficient One-Step Protocol Applicable to Microreactor Technology
    摘要:
    利用溴锂交换反应的高反应速率,通过将酮和芳基溴化物的混合物与丁基锂简单结合,可以轻松获得苯丙基醇,例如芬普类配体。
    DOI:
    10.1055/s-2008-1072771
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文献信息

  • Practical iron-catalyzed dehalogenation of aryl halides
    作者:Waldemar Maximilian Czaplik、Sabine Grupe、Matthias Mayer、Axel Jacobi von Wangelin
    DOI:10.1039/c0cc01980a
    日期:——
    An operationally simple iron-catalyzed hydrodehalogenation of aryl halides has been developed with 1 mol% Fe(acac)3 and commercial t-BuMgCl as reductant. The mild reaction conditions (THF, 0 °C, 1.5 h) effect rapid chemoselective dehalogenation of (hetero)aryl halides (I, Br, Cl) and tolerate F, Cl, OR, SR, CN, CO2R, and vinyl groups.
    开发了一种操作简便的铁催化的芳基卤化物氢脱卤反应,使用1 mol%的Fe(acac)3和商业化的t-BuMgCl作为还原剂。温和的反应条件(THF溶剂,0°C,1.5小时)实现了(杂)芳基卤化物(碘、溴、氯)的快速化学选择性脱卤,并能耐受氟、氯、烷氧基、硫醚、氰基、羧酸酯和乙烯基等官能团。
  • Synthesis and Applications of 3-[6-(Hydroxymethyl)pyridin-2-yl]-1,1′-bi-2-naphthols or 3,3′-Bis[6-(hydroxymethyl)pyridin-2-yl]-1,1′-bi-2-naphthols
    作者:Lian-Xun Gao、Li Ma、Rin-Zhe Jin、Guang-Hua Lü、Zhen Bian、Meng-Xian Ding
    DOI:10.1055/s-2007-983787
    日期:2007.8
    A series of new 1,1'-bi-2-naphthol (BINOL) derived ligands, 3-[6-(hydroxymethyl)pyridin-2-yl]-BINOLs or 3,3'-bis[6(hydroxymethyl)pyridin-2-yl]-BINOLs, bearing one or two chiral pyridinylmetlianols attached to a binaphthyl skeleton, have been synthesized using the Suzuki cross-coupling reaction. The resulting compounds have been used as ligands in the enantioselective addition of diethylzinc to aldehydes;
    一系列新的 1,1'-bi-2-naphthol (BINOL) 衍生配体,3-[6-(羟甲基)pyridin-2-yl]-BINOLs 或 3,3'-bis[6(hydroxymethyl)pyridin-已经使用 Suzuki 交叉偶联反应合成了 2-基]-BINOL,其带有一个或两个与联萘骨架相连的手性吡啶基金属醇。所得化合物已用作二乙基锌与醛的对映选择性加成的配体;获得的产品具有高达 96% 的 ee。
  • Chiral bipyridine–copper(I) complex-catalyzed enantioselective allylic oxidation of cyclic alkenes
    作者:Wing-Sze Lee、Hoi-Lun Kwong、Hoi-Ling Chan、Wing-Wai Choi、Lai-Yuen Ng
    DOI:10.1016/s0957-4166(01)00160-4
    日期:2001.5
    Chiral copper(I) bipyridine complexes were prepared and used as catalysts in the enantioselective allylic oxidation of cyclic alkenes with tert-butyl perbenzoate. The yields ranged From moderate to good and enantioselectivities up to 70% were observed. (C) 2001 Elsevier Science Ltd. All rights reserved.
  • Butyllithium-Mediated Coupling of Aryl Bromides with Ketones under In-Situ-Quench (ISQ) Conditions: An Efficient One-Step Protocol Applicable to Microreactor Technology
    作者:Hans-Günther Schmalz、Sachio Goto、Janna Velder、Sherif El Sheikh、Yuki Sakamoto、Masatoshi Mitani、Said Elmas、Andreas Adler、Anne Becker、Jörg-Martin Neudörfl、Johann Lex
    DOI:10.1055/s-2008-1072771
    日期:2008.5
    Exploiting the high rate of bromine-lithium exchange reactions, aryl carbinols such as fenpy-type ligands are readily obtained by simply combining a mixture of a ketone and an aryl bromide with butyllithium.
    利用溴锂交换反应的高反应速率,通过将酮和芳基溴化物的混合物与丁基锂简单结合,可以轻松获得苯丙基醇,例如芬普类配体。
  • New chiral 2,2′-bipyridine diols as catalysts for enantioselective addition of diethylzinc to benzaldehyde
    作者:Hoi-Lun Kwong、Wing-Sze Lee
    DOI:10.1016/s0957-4166(99)00399-7
    日期:1999.9
    New C-2-symmetric chiral 2,2'-bipyridine diols were prepared from readily available homochiral materials such as menthone and camphor. Their catalytic activities in the reaction of diethylzinc with benzaldehyde to give 1-phenyl-1-propanol were studied. In all cases, the yields were good and enantioselectivities up to 95% were observed. (C) 1999 Elsevier Science Ltd. All rights reserved.
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