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(2R,4R,4aR,7R,8aR)-4,7-dimethyl-2-(4-bromophenyl)-octahydro-2H-chromen-4-ol | 1231954-60-1

中文名称
——
中文别名
——
英文名称
(2R,4R,4aR,7R,8aR)-4,7-dimethyl-2-(4-bromophenyl)-octahydro-2H-chromen-4-ol
英文别名
(2R,4R,4aR,7R,8aR)-2-(4-bromophenyl)-4,7-dimethyl-2,3,4a,5,6,7,8,8a-octahydrochromen-4-ol
(2R,4R,4aR,7R,8aR)-4,7-dimethyl-2-(4-bromophenyl)-octahydro-2H-chromen-4-ol化学式
CAS
1231954-60-1
化学式
C17H23BrO2
mdl
——
分子量
339.272
InChiKey
SBUVBVRUTZLYMV-JSPVNYKOSA-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):
    4.1
  • 重原子数:
    20
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    异胡薄荷醇对溴苯甲醛 在 HCl treated montmorrilonite K10 作用下, 以 neat (no solvent) 为溶剂, 反应 0.05h, 以80%的产率得到
    参考文献:
    名称:
    An Environmentally Benign Synthesis of Octahydro-2H-chromen-4-ols via Modified Montmorillonite K10 Catalyzed Prins Cyclization Reaction
    摘要:
    (-)-异橙花叔醇在含有20%酸处理的蒙脱土K10催化下,能够在无溶剂条件下发生Prins环化反应,生成八氢-2H-色原-4-醇,具有良好的产率和高的顺式选择性。该固体酸催化剂在循环使用过程中不会失去活性。
    DOI:
    10.1055/s-0032-1316915
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文献信息

  • Influenza antiviral activity of F- and OH-containing isopulegol-derived octahydro-2H-chromenes
    作者:Irina V. Ilyina、Oksana S. Patrusheva、Vladimir V. Zarubaev、Maria A. Misiurina、Alexander V. Slita、Iana L. Esaulkova、Dina V. Korchagina、Yuri V. Gatilov、Sophia S. Borisevich、Konstantin P. Volcho、Nariman F. Salakhutdinov
    DOI:10.1016/j.bmcl.2020.127677
    日期:2021.1
    We synthesized fluoro- and hydroxy-containing octahydro-2H-chromenes by the Prins reaction starting from a monoterpenoid (-)-isopulegol and a wide range of aromatic aldehydes in the presence of the BF3∙Et2O/H2O system acting as both an acid catalyst and a fluorine source. Activity of the produced compounds against the influenza A/Puerto Rico/8/34 (H1N1) virus was studied. The highest activity was demonstrated by fluoro- (11i) and hydroxy-containing (10i) derivatives of 2,4,6-trimethoxybenzaldehyde. The most pronounced virus-inhibiting effect of compounds 10i and 11i was observed at an early stage of infection. These compounds were supposed to be capable of binding to viral hemagglutinin, which is an agreement with data on the effect of compounds 10i and 11i on the viral fusogenic activity as well as by molecular docking studies.
  • Sc(OTf)3-catalyzed one-pot ene-Prins cyclization: a novel synthesis of octahydro-2H-chromen-4-ols
    作者:J.S. Yadav、B.V. Subba Reddy、A.V. Ganesh、G.G.K.S. Narayana Kumar
    DOI:10.1016/j.tetlet.2010.03.100
    日期:2010.6
    (R)-Citronellal undergoes initial ene reaction followed by Prins cyclization with aldehydes in the presence of 5 mol % of scandium triflate at ambient temperature to furnish octahydro-2H-chromen-4-ols in good yields and with high cis-selectivity. The use of scandium triflate makes this procedure simple, more convenient, and practical. (C) 2010 Elsevier Ltd. All rights reserved.
  • An Environmentally Benign Synthesis of Octahydro-2H-chromen-4-ols via Modified Montmorillonite K10 Catalyzed Prins Cyclization Reaction
    作者:Gakul Baishya、Barnali Sarmah、Nabajyoti Hazarika
    DOI:10.1055/s-0032-1316915
    日期:——
    (-)-Isopulegol undergoes Prins cyclization reaction in the presence of 20 wt% of acid-treated montmorillonite K10 to produce octahydro-2H-chromen-4-ols in good yields and with high cis selectivities under solvent-free conditions. The solid-acid catalyst can be reused without loss of its activity.
    (-)-异橙花叔醇在含有20%酸处理的蒙脱土K10催化下,能够在无溶剂条件下发生Prins环化反应,生成八氢-2H-色原-4-醇,具有良好的产率和高的顺式选择性。该固体酸催化剂在循环使用过程中不会失去活性。
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