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4-(1-Propyl-butyl)-phenol | 6465-71-0

中文名称
——
中文别名
——
英文名称
4-(1-Propyl-butyl)-phenol
英文别名
4-(Heptan-4-yl)phenol;4-heptan-4-ylphenol
4-(1-Propyl-butyl)-phenol化学式
CAS
6465-71-0
化学式
C13H20O
mdl
MFCD20489522
分子量
192.301
InChiKey
RXSSFYKTUVCUKA-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

物化性质

  • 熔点:
    61-64 °C
  • 沸点:
    158-159 °C(Press: 19 Torr)
  • 密度:
    0.942±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.1
  • 重原子数:
    14
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.538
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 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
  • 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:
    4-(1-Propyl-butyl)-phenol硝酸 作用下, 以 四氯化碳 为溶剂, 生成 2,6-Dinitro-4-(1-propylbutyl)-phenol
    参考文献:
    名称:
    二硝基苯酚衍生物的结构和杀虫活性。第四部分 某些2-(α-支链烷基)-4,6-二硝基和4-(α-支链烷基)-2,6-二硝基苯酚的制备
    摘要:
    通过在醚中缩合2-或4-合成21个2-(α-支链烷基)酚和31个烷基(含5至13个碳原子)的4-(α-支链烷基)酚。酰基苯酚或更易溶的茴香醚与烷基溴化镁的混合物,脱水成烯基衍生物,进行氢化,并在需要时将苯甲醚脱甲基。2-和4-烷基苯酚转化为2-烷基- 4,6-二硝基和4-烷基- 2,6-二硝基酚,用于测试针对苹果的白粉病的致病剂白叉丝单囊壳(埃尔。和大麦Erysiphe graminisMérat和黄瓜Erysiphe cichoracearumMérat的Salm.。
    DOI:
    10.1039/j39670002281
  • 作为产物:
    描述:
    4'-甲氧基苯丁酮 在 palladium on activated charcoal 氢溴酸氢气 作用下, 以 乙醇溶剂黄146 为溶剂, 生成 4-(1-Propyl-butyl)-phenol
    参考文献:
    名称:
    二硝基苯酚衍生物的结构和杀虫活性。第四部分 某些2-(α-支链烷基)-4,6-二硝基和4-(α-支链烷基)-2,6-二硝基苯酚的制备
    摘要:
    通过在醚中缩合2-或4-合成21个2-(α-支链烷基)酚和31个烷基(含5至13个碳原子)的4-(α-支链烷基)酚。酰基苯酚或更易溶的茴香醚与烷基溴化镁的混合物,脱水成烯基衍生物,进行氢化,并在需要时将苯甲醚脱甲基。2-和4-烷基苯酚转化为2-烷基- 4,6-二硝基和4-烷基- 2,6-二硝基酚,用于测试针对苹果的白粉病的致病剂白叉丝单囊壳(埃尔。和大麦Erysiphe graminisMérat和黄瓜Erysiphe cichoracearumMérat的Salm.。
    DOI:
    10.1039/j39670002281
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文献信息

  • Site-Specific Oxidation of (sp<sup>3</sup>)C–C(sp<sup>3</sup>)/H Bonds by NaNO<sub>2</sub>/HCl
    作者:Jianyou Zhao、Tong Shen、Zhihui Sun、Nengyong Wang、Le Yang、Jintao Wu、Huichao You、Zhong-Quan Liu
    DOI:10.1021/acs.orglett.1c01303
    日期:2021.5.21
    (sp3)C–C(sp3) and (sp3)C–H bonds in aryl alkanes by the use of NaNO2/HCl was explored. The method is chemical-oxidant-free, transition-metal-free, uses water as the solvent, and proceeds under mild conditions, making it valuable and attractive to synthetic organic chemistry.
    通过使用NaNO 2 / HCl ,对芳基烷烃中的(sp 3)C–C(sp 3)和(sp 3)C–H键进行了位点特异性氧化的研究。该方法无化学氧化剂,无过渡金属,以水为溶剂,在温和条件下进行,使其对合成有机化学有价值且具有吸引力。
  • ISOCYANATE PRODUCTION PROCESS
    申请人:Shinohata Masaaki
    公开号:US20110092731A1
    公开(公告)日:2011-04-21
    An object of the present invention is to provide a process that enables isocyanate to be produced stably over a long period of time and at high yield without encountering problems of the prior art during production of isocyanate without using phosgene. The present invention discloses a process for producing an isocyanate by subjecting a carbamic acid ester to a thermal decomposition reaction, including the steps of: recovering a low boiling point component in a form of a gaseous phase component from a thermal decomposition reaction vessel in which the thermal decomposition reaction is carried out; recovering a liquid phase component containing a carbamic acid ester from a bottom of the thermal decomposition reaction vessel; and supplying all or a portion of the liquid phase component to an upper portion of the thermal decomposition reaction vessel.
    本发明的一个目的是提供一种能够在长时间内稳定地高产且不使用光气的情况下生产异氰酸酯的方法,而不会遇到先前生产异氰酸酯时的问题。本发明公开了一种通过将氨基甲酸酯经受热分解反应来生产异氰酸酯的方法,包括以下步骤:从进行热分解反应的反应釜中回收形成气相组分的低沸点组分;从热分解反应釜底部回收含有氨基甲酸酯的液相组分;并将全部或部分液相组分供给至热分解反应釜的上部。
  • PROCESS FOR PRODUCING ISOCYANATES USING DIARYL CARBONATE
    申请人:Shinohata Masaaki
    公开号:US20110054211A1
    公开(公告)日:2011-03-03
    An object of the present invention is to provide a process that enables isocyanate to be produced stably over a long period of time and at high yield without encountering problems of the prior art during production of isocyanate without using phosgene. The present invention provides an isocyanate production process including the steps of: obtaining a reaction mixture containing an aryl carbamate having an aryl group originating in a diaryl carbonate, an aromatic hydroxy compound originating in a diaryl carbonate, and a diaryl carbonate, by reacting a diaryl carbonate and an amine compound in the presence of a reaction solvent in the form of an aromatic hydroxy compound; transferring the reaction mixture to a thermal decomposition reaction vessel; and obtaining isocyanate by applying the aryl carbamate to a thermal decomposition reaction, wherein the reaction vessel in which the reaction between the diaryl carbonate and the amine compound is carried out and the thermal decomposition reaction vessel for the aryl carbamate are different.
    本发明的一个目的是提供一种能够在生产异氰酸酯时在长时间内稳定地且高产率地生产异氰酸酯的方法,而不使用光气时遇到先前技术问题的方法。本发明提供了一种异氰酸酯生产方法,包括以下步骤:通过在反应溶剂形式的芳香羟基化合物存在下,通过反应二芳基碳酸酯和胺化合物得到含有源自二芳基碳酸酯的芳基碳酸酯、源自二芳基碳酸酯的芳香羟基化合物和二芳基碳酸酯的反应混合物;将反应混合物转移至热分解反应容器;通过将芳基碳酸酯应用于热分解反应来获得异氰酸酯,其中进行二芳基碳酸酯和胺化合物之间的反应的反应容器和用于芳基碳酸酯的热分解反应的反应容器是不同的。
  • Metal cation-exchanged montmorillonite (Mn+-mont)-catalysed aromatic alkylation with aldehydes and ketones
    作者:Jun-ichi Tateiwa、Ei Hayama、Takahiro Nishimura、Sakae Uemura
    DOI:10.1039/a701744h
    日期:——
    The alkylation of aromatic compounds with aldehydes and ketones in the presence of a variety of metal cation-exchanged montmorillonites (Mn+-mont; Mn+ = Zr4+, Al3+, Fe3+, Zn2+, H+, Na+) has been investigated. Al3+- and Zr4+-Monts are revealed to be effective as catalysts, while no reaction takes place with Na+-mont. Al3+-Mont-catalysed alkylation of phenol with several aldehydes produces mainly or almost solely the corresponding gem-bis(hydroxyphenyl)alkanes (bisphenols) in good yields, while that with several ketones affords selectively the corresponding alkylphenols in moderate to good yields. The alkylation always occurs at the carbonyl carbon without any skeletal rearrangement and the kind of products depends much on the steric hindrance of an electrophilic intermediary carbocation. The alkylation of anisole, veratrole and p-cresol proceeds well, while that of toluene, benzene, chlorobenzene and nitrobenzene scarcely occurs.
    在各种金属阳离子交换的蒙脱石(Mn+-mont;Mn+ = Zr4+、Al3+、Fe3+、Zn2+、H+、Na+)存在下,研究了芳香化合物与醛和酮的烷基化反应。发现Al3+和Zr4+蒙脱石是有效的催化剂,而Na+蒙脱石则不发生反应。由Al3+蒙脱石催化的苯酚与几种醛的烷基化反应主要或几乎只生成了相应的双(羟苯基)烷烃(双酚),产率良好;而与几种酮的烷基化反应则选择性地生成了相应的烷基苯酚,产率适中至良好。烷基化总是发生在羰基碳上,没有骨架重排,产物的类型很大程度上取决于亲电中间体的碳正离子的空间位阻。茴香醚、邻苯二甲醚和对甲酚的烷基化反应良好进行,而甲苯、苯、氯苯和硝基苯的烷基化反应几乎不发生。
  • Revision of species of the “<i>Oligia</i>” <i>semicana</i> group (Lepidoptera: Noctuidae) with descriptions of a new genus and 12 new species
    作者:James T. Troubridge、J. Donald Lafontaine
    DOI:10.4039/ent134157-2
    日期:2002.4
    Abstract

    The name Neoligiagen.nov. is proposed for the “Oligiasemicana (Walker) species group in North America and 12 species, N. rubirena sp.nov., N. pagosa sp.nov., N. hardwicki sp.nov., N. inermis sp.nov., N. invenusta sp.nov., N. albirena sp.nov., N. lancea sp.nov., N. elephas sp.nov., N. lillooet sp.nov., N. surdirena sp.nov., N. canadensis sp.nov., and N. atlantica sp.nov. are described. Hadenella laevigata Smith is synonymized (synonymy restored) under Hadena tonsa Grote and Hadena hausta Grote is synonymized (synonymy restored) under Miana semicana Walker. Adults of all species are illustrated as well as male and female genitalia, where known.

    AbstractThe name Neoligiagen.nov. is proposed for the "Oligia" semicana (Walker) species group in North America and 12 species, N. rubirena sp.nov., N. pagosa sp.nov., N. hardwicki sp.nov、N. inermis sp.nov.、N. invenusta sp.nov.、N. albirena sp.nov.、N. lancea sp.nov.、N. elephas sp.nov.、N. lillooet sp.nov.、N. surdirena sp.nov.、N. canadensis sp.nov.和 N. atlantica sp.nov.等 12 个种。Hadenella laevigata Smith 与 Hadena tonsa Grote 同源(同义恢复),Hadena hausta Grote 与 Miana semicana Walker 同源(同义恢复)。所有物种的成体以及已知的雄性和雌性生殖器均附有插图。
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