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2-cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane 2-oxide

中文名称
——
中文别名
——
英文名称
2-cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane 2-oxide
英文别名
2-Cyclohexyl-4,4,5,5-tetramethyl-1,3,2lambda5-dioxaphospholane 2-oxide;2-cyclohexyl-4,4,5,5-tetramethyl-1,3,2λ5-dioxaphospholane 2-oxide
2-cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane 2-oxide化学式
CAS
——
化学式
C12H23O3P
mdl
——
分子量
246.287
InChiKey
UIDOORUCJFHYSA-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):
    2.3
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4,4,5,5-tetramethyl<1,3,2>dioxaphospholane-2-oxide环己烯2-双环己基膦-2',6'-二甲氧基联苯 、 palladium diacetate 作用下, 以 1,4-二氧六环 为溶剂, 反应 12.0h, 以70%的产率得到2-cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane 2-oxide
    参考文献:
    名称:
    钯催化链烷烃与膦酸二烷基酯的羰基化羰基化反应
    摘要:
    AbstractThe palladium‐catalyzed hydrophosphonylation of alkenes with previously unreactive acyclic dialkyl H‐phosphonates has been developed. A catalyst system based on palladium/DavePhos or palladium/SPhos enables the transformation of various alkenes to phosphonates in moderate to good yields and with excellent levels of regioselectivity. Hydrophosphonylations with internal, disubstituted and/or unactivated alkenes are also reported.magnified image
    DOI:
    10.1002/adsc.201400190
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文献信息

  • Processes for the preparation of phosphonic esters
    申请人:——
    公开号:US20030105345A1
    公开(公告)日:2003-06-05
    The present invention relates to a new manufacturing method for phosphonate esters, which have utility as a carbon-carbon binding formation agent, as well as a synthesis intermediate for biologically active substances such as medical drugs and agri-chemicals. Specifically the present invention relates to a new industrially advantageous manufacturing method for phosphonate esters in which the phosphonate esters of the subject can be efficiently obtained with a high yield rate through a simple operation while having barely any side reaction or sub-product. More specifically, the present invention pertains to a manufacturing method for phosphonate esters in which secondary phosphonate esters and alkene compounds are reacted in a transition metal medium. In addition the present invention relates to a new manufacturing method for allylphosphonate esters in which secondary cyclic phosphonate esters and 1,3-diene compounds are reacted in a palladium medium.
    本发明涉及一种新的膦酸酯制造方法,膦酸酯可用作碳碳结合形成剂,也可用作生物活性物质(如医疗药物和农用化学品)的合成中间体。 具体地说,本发明涉及一种新的具有工业优势的膦酸酯制造方法,在该方法中,可以通过简单的操作以高产率有效地获得主题的膦酸酯,同时几乎没有任何副反应或副产品。 更具体地说,本发明涉及一种膦酸酯的制造方法,其中仲膦酸酯和烯化合物在过渡金属介质中发生反应。此外,本发明还涉及一种烯丙基膦酸酯的新制造方法,其中仲环膦酸酯和 1,3-二烯化合物在钯介质中发生反应。
  • Method for manufacturing phosphonate esters
    申请人:——
    公开号:US20040220422A1
    公开(公告)日:2004-11-04
    The present invention relates to a new manufacturing method for phosphonate esters, which have utility as a carbon-carbon binding formation agent, as well as a synthesis intermediate for biologically active substances such as medical drugs and agri-chemicals. Specifically the present invention relates to a new industrially advantageous manufacturing method for phosphonate esters in which the phosphonate esters of the subject can be efficiently obtained with a high yield rate through a simple operation while having barely any side reaction or sub-product. More specifically, the present invention pertains to a manufacturing method for phosphonate esters in which secondary phosphonate esters and alkene compounds are reacted in a transition metal catalyst. In addition the present invention relates to a new manufacturing method for allylphosphonate esters in which secondary cyclic phosphonate esters and 1,3-diene compounds are reacted in a palladium catalvst.
    本发明涉及一种新的膦酸酯制造方法,膦酸酯可用作碳碳结合形成剂,也可用作生物活性物质(如医疗药物和农用化学品)的合成中间体。 具体地说,本发明涉及一种新的具有工业优势的膦酸酯制造方法,在该方法中,可以通过简单的操作以高产率有效地获得主题的膦酸酯,同时几乎没有任何副反应或副产品。 更具体地说,本发明涉及一种膦酸酯的制造方法,其中仲膦酸酯和烯化合物在过渡金属催化剂中发生反应。此外,本发明还涉及一种新的烯丙基膦酸酯制造方法,其中仲环膦酸酯和 1,3 二烯化合物在钯催化剂中发生反应。
  • High Reactivity of a Five-Membered Cyclic Hydrogen Phosphonate Leading to Development of Facile Palladium-Catalyzed Hydrophosphorylation of Alkenes
    作者:Li-Biao Han、Farzad Mirzaei、Chang-Qiu Zhao、Masato Tanaka
    DOI:10.1021/ja000444v
    日期:2000.6.1
  • PROCESSES FOR THE PREPARATION OF PHOSPHONIC ESTERS
    申请人:Japan Science and Technology Agency
    公开号:EP1195380B1
    公开(公告)日:2004-07-14
  • US6765107B2
    申请人:——
    公开号:US6765107B2
    公开(公告)日:2004-07-20
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同类化合物

(1-氨基丁基)磷酸 顺丙烯基磷酸 除草剂BUMINAFOS 阿仑膦酸 阻燃剂 FRC-1 铵甲基膦酸盐 钠甲基乙酰基膦酸酯 钆1,5,9-三氮杂环十二烷-N,N',N''-三(亚甲基膦酸) 钆-1,4,7-三氮杂环壬烷-N,N',N''-三(亚甲基膦酸) 重氮甲基膦酸二乙酯 辛基膦酸二丁酯 辛基膦酸 辛基-膦酸二钾盐 辛-1-烯-2-基膦酸 试剂12-Azidododecylphosphonicacid 英卡膦酸 苯胺,4-乙烯基-2-(1-甲基乙基)- 苯甲基膦酸二甲酯 苯基膦酸二甲酯 苯基膦酸二仲丁酯 苯基膦酸二乙酯 苯基膦酸二乙酯 苯基磷酸二辛酯 苯基二异辛基亚磷酸酯 苯基(1H-1,2,4-三唑-1-基)甲基膦酸二乙酯 苯丁酸,b-氨基-g-苯基- 苄基膦酸苄基乙酯 苄基亚甲基二膦酸 膦酸,[(2-乙基己基)亚氨基二(亚甲基)]二,triammonium盐(9CI) 膦酸叔丁酯乙酯 膦酸单十八烷基酯钾盐 膦酸二辛酯 膦酸二(二十一烷基)酯 膦酸,辛基-,单乙基酯 膦酸,甲基-,单(2-乙基己基)酯 膦酸,甲基-,二(苯基甲基)酯 膦酸,甲基-,2-甲氧基乙基1-甲基乙基酯 膦酸,丁基乙基酯 膦酸,[苯基[(苯基甲基)氨基]甲基]-,二甲基酯 膦酸,[[羟基(苯基甲基)氨基]苯基甲基]-,二(苯基甲基)酯 膦酸,[2-(环丙基氨基)-2-羰基乙基]-,二乙基酯 膦酸,[2-(二甲基亚肼基)丙基]-,二乙基酯,(E)- 膦酸,[1-甲基-2-(苯亚氨基)乙烯基]-,二乙基酯 膦酸,[1-(乙酰基氨基)-1-甲基乙基]-(9CI) 膦酸,[(环己基氨基)苯基甲基]-,二乙基酯 膦酸,[(二乙氧基硫膦基)(二甲氨基)甲基]- 膦酸,[(2S)-2-氨基-2-苯基乙基]-,二乙基酯 膦酸,[(1Z)-2-氨基-2-(2-噻嗯基)乙烯基]-,二乙基酯 膦酸,P-[(二乙胺基)羰基]-,二乙基酯 膦酸,(氨基二环丙基甲基)-