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1-butyl-3-methylimidazolium difluorohydridotris(pentafluoroethyl)phosphate | 1310495-70-5

中文名称
——
中文别名
——
英文名称
1-butyl-3-methylimidazolium difluorohydridotris(pentafluoroethyl)phosphate
英文别名
——
1-butyl-3-methylimidazolium difluorohydridotris(pentafluoroethyl)phosphate化学式
CAS
1310495-70-5
化学式
C6HF17P*C8H15N2
mdl
——
分子量
566.241
InChiKey
QECJANHZKZCAAK-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):
    7.62
  • 重原子数:
    34
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    8.8
  • 氢给体数:
    0
  • 氢受体数:
    18

反应信息

  • 作为产物:
    描述:
    tris(pentafluoroethyl)difluorophosphorane氯化(1-丁基-3-甲基咪唑) 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 反应 0.83h, 以64%的产率得到1-butyl-3-methylimidazolium difluorohydridotris(pentafluoroethyl)phosphate
    参考文献:
    名称:
    含氢磷酸根阴离子[P(C2F5)3F2H] –的稳定盐的合成
    摘要:
    工业品(C 2 F 5)3 PF 2与LiAlH 4在THF溶液中的反应选择性地提供了氢化磷酸根阴离子[P(C 2 F 5)3 F 2 H] –。通过在THF水溶液中进行盐复分解,以数克规模获得无色固体的化合物[PPh 4 ] [P(C 2 F 5)3 F 2 H]。结合[P(C 2 F 5)3 F 2 H] –与各种咪唑鎓和吡啶鎓阳离子一起使用可提供熔点远低于室温的离子液体。(C 2 F 5)3 PF 2还从胺中提取氢化物,得到氢磷酸根阴离子[P(C 2 F 5)3 F 2 H] –以及相应的亚胺阳离子,后者通过分子内或分子间加合物添加第二个胺部分编队。
    DOI:
    10.1002/ejic.201701375
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文献信息

  • COMPOUNDS WITH (PERFLUOROALKYL) FLUOROHYDROGENPHOSPHATE ANIONS
    申请人:Ignatyev Nikolai (Mykola)
    公开号:US20120264946A1
    公开(公告)日:2012-10-18
    The present invention relates to a process for the preparation of compounds with (perfluoroalkyl)fluorohydrogenphosphate anion, and to compounds containing (perfluoroalkyl)fluorohydrogenphosphate anion and to the use thereof.
    本发明涉及一种制备含有(全氟烷基)氟氢磷酸盐阴离子的化合物的方法,以及含有(全氟烷基)氟氢磷酸盐阴离子的化合物及其用途。
  • US8916729B2
    申请人:——
    公开号:US8916729B2
    公开(公告)日:2014-12-23
  • Synthesis of Stable Salts Containing the Hydridophosphate Anion [P(C <sub>2</sub> F <sub>5</sub> ) <sub>3</sub> F <sub>2</sub> H] <sup>–</sup>
    作者:Julia Bader、Nikolai Ignat'ev、Berthold Hoge
    DOI:10.1002/ejic.201701375
    日期:2018.2.21
    anion [P(C2F5)3F2H]. The compound [PPh4][P(C2F5)3F2H] is obtained as a colorless solid on a multigram scale by salt metathesis in aqueous THF. Combining [P(C2F5)3F2H] with various imidazolium and pyridinium cations affords ionic liquids with melting points well below room temperature. (C2F5)3PF2 also abstracts hydrides from amines, affording the hydridophosphate anion [P(C2F5)3F2H] and the corresponding
    工业品(C 2 F 5)3 PF 2与LiAlH 4在THF溶液中的反应选择性地提供了氢化磷酸根阴离子[P(C 2 F 5)3 F 2 H] –。通过在THF水溶液中进行盐复分解,以数克规模获得无色固体的化合物[PPh 4 ] [P(C 2 F 5)3 F 2 H]。结合[P(C 2 F 5)3 F 2 H] –与各种咪唑鎓和吡啶鎓阳离子一起使用可提供熔点远低于室温的离子液体。(C 2 F 5)3 PF 2还从胺中提取氢化物,得到氢磷酸根阴离子[P(C 2 F 5)3 F 2 H] –以及相应的亚胺阳离子,后者通过分子内或分子间加合物添加第二个胺部分编队。
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同类化合物

氯(双五氟乙基)膦 5-萘-2-基-1,3-噁唑 1-氯-2-[2-氯乙基(甲基)磷基]乙烷 1-丁基-1-甲基吡咯烷鎓三(五氟乙基)三氟磷酸盐 1,1,1,3,3,3-六氟-2-(2,2,2-三氟-1-羟基-1-(三氟甲基)乙基磷酰基)-2-丙醇 bis(pentafluoroethyl)phosphinyl amide 1-butylpyridinium bis(pentafluoroethyl)phosphinate N,N-butylmethylpyrrolidinium bis(pentafluoroethyl)-phosphinate bis(pentafluoroethyl)phosphinate anion triethylmethylammonium bis(pentafluoroethyl)-phosphinate bis(dimethylamino)chlorocarbenium bis(pentafluorethyl)phosphinate 1-methyl-1-propargylpyrrolidinium bis(pentafluoro-ethyl)phosphinate N,N-dimethylpyrrolidinium bis(pentafluoroethyl)-phosphinate 1-butyl-3-methylimidazolium bis(pentafluoroethyl)phosphinate propargyl bis(pentafluoroethyl)phosphinate 1,3-dimethylimidazolium bis(pentafluoroethyl)phosphinate 1-propargyl-3-methylimidazolium bis(pentafluoroethyl)-phosphinate 1-ethyl-3-methylimidazolium bis(nonafluorobutyl)-phosphinate tetrabutylammonium tris(pentafluoroethyl)trifluorophosphate bis-(2,2-dichloro-1-hydroxy-ethyl)-phosphinic acid 2,2,3,3,4,4,5,5-octafluoropentyl bis(pentafluoroethyl) phosphinate 2-methyl-1,1,3,3-tetramethylisouronium bis(pentafluoroethyl)phosphinate ethyl bis(nonafluorobutyl)phosphinate fluorobis(pentafluoroethyl)phosphane tetraethylammonium bis(nonafluorobutyl)tetrafluorophosphate tetraethylammonium tris(pentafluoroethyl)trifluorophosphate tris(pentafluoroethyl)phosphane ethyl bis(pentafluoroethyl)phosphinate N,N,N',N'-tetramethyl-N''-ethylguanidinium bis(pentafluoroethyl)phosphinate 3-bromopropyl bis(pentafluoroethyl)phosphinate Tetramethylammonium tris(pentafluorophosphate Bis-(2-chlor-ethyl)-thiophosphinsaeure-ethylester ethyl bis(pentafluoroethyl)phosphinite Bis-heptafluorpropyl-fluorphosphin trimethylsilyl bis(pentafluoroethyl)phosphinite tris(undecafluoroisopentyl)phosphine oxide 1-(Bis-undecafluoropentyl-phosphinoyl)-1,1,2,2,3,3,4,4,5,5,5-undecafluoro-pentane Bis-(2-chlor-ethyl)-chlorphosphin 1,1,1,3,3,3,1',1',1',3',3',3'-dodecafluoro-2,2'-phosphanediyl-bis-propan-2-ol Bis-<2-chlor-aethyl>-chlormethyl-phosphinoxid Tri(β-chlorethyl)phosphinoxid cis-[(C2F5)2P(methyl)]4Pt Perfluorhexylphosphinsaeure bis-(2,2,2-trichloro-1-hydroxy-ethyl)-phosphinic acid ethyl ester bis(pentafluoroethyl)phosphinyl bromide (S)-4-benzyl-2-(2-(bis(pentafluoroethyl)phosphino)phenyl)-4,5-dihydrooxazole (S)-2-(2-(bis(pentafluoroethyl)phosphino)phenyl)-4-phenyl-4,5-dihydrooxazole tetra(n-butyl)phosphonium tris(pentafluoroethyl)trifluorophosphate silver bis(heptafluoropropyl)phosphinate Tris(2,2,3,3,4,4,5,5-octafluoropentyl)phosphine