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(1-fluoroheptyl)benzene | 1428331-74-1

中文名称
——
中文别名
——
英文名称
(1-fluoroheptyl)benzene
英文别名
1-Fluoroheptylbenzene
(1-fluoroheptyl)benzene化学式
CAS
1428331-74-1
化学式
C13H19F
mdl
——
分子量
194.292
InChiKey
CSACECFBNJQROP-UHFFFAOYSA-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):
    5
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    庚基苯iron(II) acetylacetonate 、 Selectfluor 作用下, 以 乙腈 为溶剂, 反应 24.0h, 以68%的产率得到(1-fluoroheptyl)benzene
    参考文献:
    名称:
    Iron(II)-Catalyzed Benzylic Fluorination
    摘要:
    Direct C-F functionalization of benzylic sp(3) C-H bonds is a synthetic challenge that has yet to be propitiously overcome. A mild, one-pot synthesis of monofluorinated benzylic substrates is reported with commercially available iron(II) acetylacetonate and Selectfluor in good to excellent yields and selectivity. A convenient route to beta-fluorinated products of 3-aryl ketones is also highlighted, providing a synthetic equivalent to the difficult to accomplish conjugate addition of fluoride to alpha,beta-unsaturated ketones.
    DOI:
    10.1021/ol400424s
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文献信息

  • Silver-Catalyzed Decarboxylative Alkylfluorination of Alkenes
    作者:Chen-Guang Li、Qiang Xie、Xiao-Lan Xu、Feng Wang、Bei Huang、Yu-Feng Liang、Hua-Jian Xu
    DOI:10.1021/acs.orglett.9b03381
    日期:2019.10.18
    with the catalysis of silver(I) and Selectfluor as both the oxidant and fluorine source. This reaction is highly chemoselective, producing the decarboxylative alkylfluorination products rather than the competitive fluorination of aliphatic carboxylic acids. This practical transformation proceeds efficiently in aqueous media at room temperature and exhibits a large range of functional-group tolerance
    (I)和Selectfluor作为氧化剂和源的催化作用,开发了用于烷基烯烃化的烷基羧酸脱羧剂。该反应是高度化学选择性的,产生脱羧烷基化产物,而不是脂肪族羧酸的竞争性化。这种实际的转变在室温下在性介质中有效地进行,并且在各种伯和仲脂肪族羧酸盐和烯烃中表现出大范围的官能团耐受性。
  • Method for producing an aromatic compound having an alkyl group with at least three carbon atoms
    申请人:TORAY INDUSTRIES, INC.
    公开号:EP0985649A2
    公开(公告)日:2000-03-15
    Aromatic compounds having an alkyl group with at least 3 carbon atoms are produced in a process comprising at least one of the following steps: (1) a step of contacting a starting material that contains an aromatic compound having a branched alkyl group with at least 3 carbon atoms, with a zeolite-containing catalyst in a liquid phase in the presence of hydrogen therein, thereby changing the position of the carbon atoms of the alkyl group bonding to the aromatic ring of the compound; (2) a step of contacting a starting material that contains an aromatic compound having a branched alkyl group with at least 3 carbon atoms, with a catalyst containing zeolite and containing rhenium and/or silver, in a liquid phase, thereby changing the position of the carbon atoms of the alkyl group bonding to the aromatic ring of the compound; (3) a step of contacting a halogenated aromatic compound having an alkyl group with at least 3 carbon atoms, with an acid-type catalyst, thereby isomerizing the compound; and (4) a step of treating a mixture of isomers of an aromatic compound having an alkyl group with at least 3 carbon atoms, with a zeolite adsorbent that contains at least one exchangable cation selected from alkali metals, alkaline earth metals, lead, thallium and silver, thereby separating a specific isomer from the isomer mixture through adsorption.
    具有至少 3 个碳原子烷基的芳香族化合物的生产工艺至少包括以下一个步骤: (1) 将含有至少 3 个碳原子的支链烷基的芳香族化合物的起始原料在液相中与含沸石的催化剂在氢存在的情况下接触,从而改变烷基的碳原子与化合物的芳香环键合的位置; (2) 将含有芳香族化合物的起始原料与含沸石和含和/或的催化剂在液相中接触,该芳香族化合物具有至少 3 个碳原子的支链烷基,从而改变烷基碳原子与化合物芳香环键合的位置; (3) 将具有至少 3 个碳原子的烷基的卤代芳香族化合物与酸型催化剂接触,从而使该化合物异构化;以及 (4) 用沸石吸附剂处理具有至少 3 个碳原子的烷基的芳香族化合物的异构体混合物,该沸石吸附剂含有至少一种选自碱属、碱土属、的可交换阳离子,从而通过吸附从异构体混合物中分离出特定的异构体。
  • US6462248B1
    申请人:——
    公开号:US6462248B1
    公开(公告)日:2002-10-08
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