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5-allyl-1,1,2,2,3,3,4,4-octafluoropentyl ether

中文名称
——
中文别名
——
英文名称
5-allyl-1,1,2,2,3,3,4,4-octafluoropentyl ether
英文别名
5,5,6,6,7,7,8,8-Octafluoro-8-(1,1,2,2,3,3,4,4-octafluorooct-7-enoxy)oct-1-ene;5,5,6,6,7,7,8,8-octafluoro-8-(1,1,2,2,3,3,4,4-octafluorooct-7-enoxy)oct-1-ene
5-allyl-1,1,2,2,3,3,4,4-octafluoropentyl ether化学式
CAS
——
化学式
C16H14F16O
mdl
——
分子量
526.261
InChiKey
NVZIPTGMZJQVOC-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):
    8.6
  • 重原子数:
    33
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    17

反应信息

  • 作为产物:
    描述:
    2,2,3,3,4,4,5,5-八氟-1-戊醇3-氯丙烯 在 potassium hydroxide 作用下, 以 乙腈 为溶剂, 反应 30.5h, 以89%的产率得到5-allyl-1,1,2,2,3,3,4,4-octafluoropentyl ether
    参考文献:
    名称:
    一种高效,无溶剂的催化方法,用于合成单有机官能化的1,1,3,3-四甲基二硅氧烷衍生物
    摘要:
    报道了通过氢化硅烷化反应用烯烃对1,1,3,3-四甲基二硅氧烷(TMDSO)的选择性单官能化。在对TMDSO与选定的含C = C键的烯烃之间的反应中铂和铑配合物进行研究的基础上,可以选择最有效的催化剂,其在无溶剂体系中的应用会导致选择性的单官能化二硅氧烷试剂并仅同时形成β-区域异构产物,它们的结构官能团具有独特的反应性或物理化学性质。
    DOI:
    10.1016/j.jorganchem.2017.06.025
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文献信息

  • [EN] SYNTHESIS OF FLUOROCARBOFUNCTIONAL ALKOXYSILANES AND CHLOROSILANES<br/>[FR] SYNTHÈSE D'ALCOXYSILANES ET CHLOROSILANES À FONCTION FLUOROCARBO
    申请人:UNIV ADAM MICKIEWICZ
    公开号:WO2011028141A1
    公开(公告)日:2011-03-10
    The subject of invention is the method of synthesis of fluorocarbofunctional alkoxysilanes and chlorosilanes of the general formula HCF2(CF2)n(CH2)mOC3H7SiR1R2R3 in which - n takes values from 1 to 12, m takes values from 1 to 4, - R1 stands for an alkoxy group or halogen, if R1 stands for an alkoxy group, then R2 and R3 can be the same or different and stand for an alkoxy group containing C= 1-4, alkyl group containing C = 1-12 or an aryl group, if R1 stands for a halogen, then R2 and R3 can be the same or different and stand for based on hydrosilylation of an appropriate fluoroalkyl-allyl ether with an appropriate trisubstituted silane of the general formula HSiR1R2R3 in the presence of siloxide rhodium complex [Rh(OSiMe3)(cod)}2] as a catalyst.
    发明的主题是通式HCF2(CF2)n(CH2)mOC3H7SiR1R2R3的氟碳功能性烷氧基硅烷和氯硅烷的合成方法,其中- n的值为1至12,m的值为1至4,- R1代表烷氧基团或卤素,如果R1代表烷氧基团,则R2和R3可以相同也可以不同,并且代表含有C=1-4的烷氧基团,含有C=1-12的烷基团或芳基,如果R1代表卤素,则R2和R3可以相同也可以不同,并且基于适当的氟烷基烯醚与通式HSiR1R2R3的适当三取代硅烷之间的氢硅烷化反应,在硅氧烷钌配合物[Rh(OSiMe3)(cod)}2]存在下作为催化剂。
  • SYNTHESIS OF FLUOROCARBOFUNCTIONAL ALKOXYSILANES AND CHLOROSILANES
    申请人:Marciniec Bogdan
    公开号:US20120165565A1
    公开(公告)日:2012-06-28
    The subject of invention is the method of synthesis of fluorocarbofunctional alkoxysilanes and chlorosilanes of the general formula HCF 2 (CF 2 ) n (CH 2 ) m OC 3 H 7 SiR 1 R 2 R 3 in which -n takes values from 1 to 12, m takes values from 1 to 4,—R 1 stands for an alkoxy group or halogen, if R 1 stands for an alkoxy group, then R 2 and R 3 can be the same or different and stand for an alkoxy group containing C=1-4, alkyl group containing C=1-12 or an aryl group, if R 1 stands for a halogen, then R 2 and R 3 can be the same or different and stand for based on hydrosilylation of an appropriate fluoroalkyl-allyl ether with an appropriate trisubstituted silane of the general formula HSiR 1 R 2 R 3 in the presence of siloxide rhodium complex [Rh(OSiMe 3 )(cod)} 2 ] as a catalyst.
    发明的主题是通式HCF2(CF2)n(CH2)mOC3H7SiR1R2R3的氟碳功能烷氧基硅烷和氯硅烷的合成方法,其中-n的值为1至12,m的值为1至4,-R1代表烷氧基或卤素,如果R1代表烷氧基,则R2和R3可以相同也可以不同,并且代表含有C=1-4的烷氧基、含有C=1-12的烷基或芳基,如果R1代表卤素,则R2和R3可以相同也可以不同,并且基于适当的氟烷基烯醚与通式HSiR1R2R3的适当三取代硅烷之间的氢硅烷基化反应,在催化剂[Rh(OSiMe3)(cod)}2]存在下进行。
  • SYNTHESIS OF FLUOROCARBOFUNCTIONAL SILSESQUIOXANES
    申请人:Marciniec Bogdan
    公开号:US20120157702A1
    公开(公告)日:2012-06-21
    The subject of the invention is the method of synthesis of fluoracarbofunctional cage silsesquioxanes of the general formula in which • R 1 stands for HCF 2 (CF 2 ) n (CH 2 )mO(CH 2 ) 3 Si(CH 3 ) 2 O or HCF 2 (CF 2 ) n (CH 2 ) m O(CH 2 ) 3 group in which n=1-12, m=1-4; • R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 can be the same as R 1 or different from it and stand all either for the (C 1 -C 25 ) alkyl group or any aryl group, based on hydrosilylation of fluoroalkyl-allyl ether with an appropriate hydrogen-silsesquioxane in the presence of siloxide rhodium complex [Rh(OSiMe 3 )(cod)} 2 ] as a catalyst.
    本发明的主题是合成通式为的氟碳功能笼状倍半硅氧烷的方法,其中 • R1代表HCF2(CF2)n(CH2)mO(CH2)3Si(CH3)2O或HCF2(CF2)n(CH2)mO(CH2)3基团,其中n=1-12,m=1-4; • R2,R3,R4,R5,R6,R7,R8可以与R1相同或不同,并且全部代表(C1-C25)烷基或任何芳基,基于氢硅烷与适当的氟烷基烯丙醚在硅氧化物铑配合物[Rh(OSiMe3)(cod)}2]存在下的氢硅化反应。
  • US8816117B2
    申请人:——
    公开号:US8816117B2
    公开(公告)日:2014-08-26
  • [EN] SYNTHESIS OF FLUOROCARBOFUNCTIONAL SILSESQUIOXANES<br/>[FR] SYNTHÈSE DE SILSESQUIOXANES À FONCTIONNALITÉ FLUOROCARBONÉE
    申请人:UNIV ADAM MICKIEWICZ
    公开号:WO2011028142A1
    公开(公告)日:2011-03-10
    The subject of the invention is the method of synthesis of fluorocarbofunctional cage silsesquioxanes of the general formula in which • R1 stands for HCF2(CF2)n(CH2)mO(CH2)3Si(CH3)2O or HCF2(CF2)n(CH2)mO(CH2)3 group in which n=1-12, m=1-4; • R2, R3, R4, R5, R6, R7, R8 can be the same as R1 or different from it and stand all either for the (C1-C25) alkyl group or any aryl group, based on hydrosilylation of fluoroalkyl-allyl ether with an appropriate hydrogensilsesquioxane in the presence of siloxide rhodium complex [Rh(OSiMe3)(cod)}2] as a catalyst.
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