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1-butyl-3-methylimidazolium bis(pentafluoroethyl)phosphinate

中文名称
——
中文别名
——
英文名称
1-butyl-3-methylimidazolium bis(pentafluoroethyl)phosphinate
英文别名
bis(1,1,2,2,2-pentafluoroethyl)phosphinate;1-butyl-3-methylimidazol-3-ium
1-butyl-3-methylimidazolium bis(pentafluoroethyl)phosphinate化学式
CAS
——
化学式
C4F10O2P*C8H15N2
mdl
——
分子量
440.221
InChiKey
CCMGWQKKOYVFNL-UHFFFAOYSA-M
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):
    4.05
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    48.9
  • 氢给体数:
    0
  • 氢受体数:
    12

反应信息

  • 作为产物:
    描述:
    methyl ester of bis(pentafluoroethyl)phosphinic acid氯化(1-丁基-3-甲基咪唑) 25.0~90.0 ℃ 、1.77 kPa 条件下, 反应 8.5h, 以giving 1.74 g of 1-butyl-3-methylimidazolium bis(pentafluoroethyl)phosphinate as a liquid的产率得到1-butyl-3-methylimidazolium bis(pentafluoroethyl)phosphinate
    参考文献:
    名称:
    PROCESS FOR THE PREPARATION OF ONIUM SALTS WITH DIALKYLPHOSPHATE, DIALKYLPHOSPHINATE OR (O-ALKYL)ALKYL- OR ALKYLPHOSPHONATE ANIONS HAVING A LOW HALIDE CONTENT
    摘要:
    本发明涉及一种制备含二烷基磷酸盐、二烷基磷酸酯或(O-烷基)烷基或烷基膦酸盐阴离子的离子盐的方法,该方法通过将离子卤化物与三烯丙基磷酸酯、烷基二烷基磷酸酯、二烷基烷基膦酸酯或磷酸、二烷基膦酸或烷基膦酸的混合烷基三烷基硅酯进行反应来实现。
    公开号:
    US20090253914A1
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文献信息

  • WO2006/63655
    申请人:——
    公开号:——
    公开(公告)日:——
  • VERFAHREN ZUR HERSTELLUNG VON BIS(PERFLUORALKYL)PHOSPHINSÄUREN UND DEREN SALZE
    申请人:Merck Patent GmbH
    公开号:EP1495035B1
    公开(公告)日:2010-06-30
  • VERFAHREN ZUR HERSTELLUNG VON ONIUM-SALZEN MIT DIALKYLPHOSPHAT-, DIALKYLPHOSPHINAT- ODER (O-ALKYL)-ALKYL- ODER ALKYL-PHOSPHONAT-ANIONEN MIT GERINGEM HALOGENID-GEHALT
    申请人:Merck Patent GmbH
    公开号:EP1824866A1
    公开(公告)日:2007-08-29
  • Verfahren zur Herstellung von Onium-Salzen mit Diakylphosphinat Anionen mit geringem Halogenid-Gehalt
    申请人:Merck Patent GmbH
    公开号:EP2180002B1
    公开(公告)日:2012-12-26
  • Process for the preparation of bis(perfluoroalkyl)phosphinic acids and salts thereof
    申请人:Welz-Biermann Urs
    公开号:US20050256334A1
    公开(公告)日:2005-11-17
    The present invention relates to a process for the preparation of bis(perfluoroalkyl)phosphinic acids comprising at least the reaction of at least one difluorotris(perfluoroalkyl)phosphorane or at least one trifluorobis(perfluoroalkyl)phosphorane with hydrogen fluoride in a suitable reaction medium, and heating of the resultant reaction mixture. The invention also relates to salts of bis(perfluoroalkyl)phosphinic acids and to the use thereof.
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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