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ethyl bis(pentafluoroethyl)phosphinate

中文名称
——
中文别名
——
英文名称
ethyl bis(pentafluoroethyl)phosphinate
英文别名
1-[ethoxy(1,1,2,2,2-pentafluoroethyl)phosphoryl]-1,1,2,2,2-pentafluoroethane
ethyl bis(pentafluoroethyl)phosphinate化学式
CAS
——
化学式
C6H5F10O2P
mdl
——
分子量
330.062
InChiKey
UEVNGWWHQPOYKR-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):
    3.6
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    12

反应信息

  • 作为反应物:
    描述:
    茴香硫醚ethyl bis(pentafluoroethyl)phosphinate正己烷 为溶剂, 反应 9.0h, 以100%的产率得到ethylmethylphenylsulfonium bis(pentafluoroethyl)phosphinate
    参考文献:
    名称:
    PROCESS FOR THE PREPARATION OF PHOSPHINIC ACID ESTERS
    摘要:
    该发明涉及一种通过将相应的膦氧化物与醇或酚在碱金属氟化物或四烷基铵氟化物存在下反应制备烷基膦酸酯、烯基膦酸酯、炔基膦酸酯或苯基膦酸酯的过程。
    公开号:
    US20150045572A1
  • 作为产物:
    描述:
    bis(pentafluoroethyl)phosphinate anion乙醇四甲基氟化铵 作用下, 反应 4.5h, 以93%的产率得到ethyl bis(pentafluoroethyl)phosphinate
    参考文献:
    名称:
    PROCESS FOR THE PREPARATION OF PHOSPHINIC ACID ESTERS
    摘要:
    该发明涉及一种通过将相应的膦氧化物与醇或酚在碱金属氟化物或四烷基铵氟化物存在下反应制备烷基膦酸酯、烯基膦酸酯、炔基膦酸酯或苯基膦酸酯的过程。
    公开号:
    US20150045572A1
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文献信息

  • PROCESS FOR THE PREPARATION OF ONIUM SALTS WITH DIALKYLPHOSPHATE, DIALKYLPHOSPHINATE OR (O-ALKYL)ALKYL- OR ALKYLPHOSPHONATE ANIONS HAVING A LOW HALIDE CONTENT
    申请人:Ignatyev Nikolai (Mykola)
    公开号:US20090253914A1
    公开(公告)日:2009-10-08
    The invention relates to a process for the preparation of onium salts with dialkylphosphate, dialkylphosphinate or (O-alkyl)alkyl- or alkylphosphonate anions by reaction of an onium halide with a triallyl phosphate, alkyl dialkylphosphinate, dialkyl alkylphosphonate or trialkylsilyl ester or mixed alkyl trialkylsilyl ester of phosphoric, dialkylphosphinic or alkylphosphonic acid.
    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。
  • Process for the preparation of phosphinic acid esters
    申请人:Merck Patent GmbH
    公开号:US09056881B2
    公开(公告)日:2015-06-16
    The invention relates to a process for the preparation of alkyl phosphinates, alkenyl phosphinates, alkynyl phosphinates or phenyl phosphinates by reaction of a corresponding phosphine oxide with an alcohol or phenol in the presence of alkali-metal fluoride or tetraalkylammonium fluoride.
    本发明涉及一种制备烷基磷酸酯、烯基磷酸酯、炔基磷酸酯或苯基磷酸酯的方法,通过在碱金属氟化物或四烷基铵氟化物的存在下,将相应的膦氧化物与醇或酚反应。
  • 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
  • VERFAHREN ZUR HERSTELLUNG VON PHOSPHINSÄUREESTERN
    申请人:Merck Patent GmbH
    公开号:EP2820026A1
    公开(公告)日:2015-01-07
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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