Tris(Triphenylphosphine)Ruthenium(II) Chloride 三苯基膦氯化钌(II)

CAS 15529-49-4 MFCD00013077

化学结构图

15529-49-4
SMILES: [ClH-].[ClH-].[Ru+2].c1ccccc1P(c1ccccc1)c1ccccc1.c1ccccc1P(c1ccccc1)c1ccccc1.c1ccccc1P(c1ccccc1)c1ccccc1

化学属性

Mol. Formula[(C6H5)3P]3RuCl2
Mol. Weight959
Melting Point159°C
TSCANo
SolubilityVery slightly soluble (with dissociation) in acetone, alcohol, chloroform, ethyl acetate, and toluene
Stability对空气和湿度敏感

别名和识别编码

Chemical NameTris(Triphenylphosphine)Ruthenium(II) Chloride
Synonym 三(三苯基膦)二氯化钌(II) Dichlorotris(triphenylphosphine)ruthenium(II) Tris(triphenylphosphine)ruthenium(II)chloride Dichlorotris-(triphenylphosphin)-ruthenium(II) Tris-(triphenylphosphin)-ruthenium(II)-chlorid Dichlorotris(triphenylphosphine)ruthenium Ruthenium-tris-(triphenylphosphin)-dichlorid Tris(triphenylphosphine)ruthenium(II) chloride Tris(triphenylphosphin)-ruthenium(II)-chlorid Ruthenium tris(triphenylphosphine) dichloride Dichlorotris(triphenylphosphin)ruthenium(II) 三(三苯基膦)二氯化钌 Tris(triphenylphosphine)ruthenium dichloride Tris(triphenylphosphine)dichlororuthenium 三(三苯基膦)氯化钌(II) 三苯基膦氯化钌 Dichlortris(triphenylphosphin)ruthenium Dichlorotris(triphenylphosphin)-ruthenium(II) Dichlorotris(triphenylphosphine)ruthenium (II) Ruthenium, dichlorotris(triphenylphosphine)- Tris(triphenylphosphine)ruthenium(II) dichloride
MDL NumberMFCD00013077
PubChem Substance ID11007548
Beilstein Registry Number4935939
EC Number239-569-7
CAS Number15529-49-4
Chemical Name Translation三苯基膦氯化钌(II)
Reaxys-RN14715227
LabNetwork Molecule IDLN00192208
InChIKeyWIWBLJMBLGWSIN-UHFFFAOYSA-L
InChIInChI=1S/3C18H15P.2ClH.Ru/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h3*1-15H;2*1H;/q;;;;;+2/p-2
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分类

  • {SNA} C-H Activation, Catalysis and Inorganic Chemistry, Chemical Synthesis, Ru Catalysts, Ruthenium Catalysts
  • {SA} Catalysis and Inorganic Chemistry, Chemical Synthesis, Ru Catalysts, Ruthenium Catalysts
  • {uni_hamburg} no charge; carbocycle; aromatic; 6RingOnly; 6ring; 1fragment
  • {SNA} C-H Activation, Catalysis and Inorganic Chemistry, Catalysts, Chemical Synthesis, Ru Catalysts, Ruthenium Catalysts

产品应用

  • 1.环己烷酮生成环己烷酚
  • 2.脂肪酮生成脂肪酮
  • 3.萘甲基酮生成醇
  • Tris(triphenylphosphine)ruthenium(II) dichloride

相关文献及参考

  • In combination with ethylenediamine and KOH in 2-propanol, conventional hydrogenation of ketones can be accomplished: J. Am. Chem. Soc., 117, 2675 (1995);
  • Short: III/5b
  • In the presence of KOH, catalyzes the one-pot ɑ-alkylation of secondary alcohols with primary alcohols: Organometallics, 22, 3608 (2002).
  • Homoallylic alcohols can be isomerized to allylic: J. Am. Chem. Soc., 118, 12867 (1996); Tetrahedron, 54, 5129 (1998).
  • Versatile homogeneous isomerization, reduction and oxidation catalyst.
  • Short: EINECS
  • In the presence of acetone, secondary alcohols can be oxidized to ketones: J. Chem. Soc., Chem. Commun., 337 (1992). For use in the dehydrogenation of amines to imines and the oxidation of cyanohydrins to acyl cyanides, see tert-Butyl­ hydroperoxide, A13926. In combination with hydroquinone, selective aerobic oxidation of a primary alcohol to an aldehyde, in the presence of a secondary alcohol, can be achieved: Tetrahedron Lett., 39, 5557 (1998).
  • Catalyst for the reaction of N-alkylanilines with triethanolamine in dioxan (autoclave) to give the corresponding 1-alkylindoles in good yield: Synth. Commun., 26, 1349 (1996).
  • Catalyzes the cyclization 2-aminophenethyl alcohols to indoles in high yield: J. Org. Chem., 55, 580 (1990):
  • Alkylated arenes can be oxidized to ketones by tert-butyl hydroperoxide, catalyzed by the complex: J. Org. Chem., 65, 9186 (2000).
  • Catalyzes hydrogenation of aromatic nitro compounds to amines; selective reduction is possible in the presence of halogen, ester, nitrile and even additional nitro groups: Tetrahedron Lett., 2163 (1975). Aliphatic nitro compounds are hydrogenated to amines under high pressure: J. Org. Chem., 40, 519 (1975). Also catalyzes the high-yield reduction of nitroarenes to amines, indoles to indolines, quinolines to 1,2,3,4-tetrahydroquinolines by formic acid and triethylamine: Bull. Chem. Soc. Jpn., 57, 2440 (1984).

安全信息

WGK Germany3
GHS Symbol
Precautionary statements
  • P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
  • P304+P340+P312
  • P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
  • P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
  • P271 Use only outdoors or in a well-ventilated area.? 只能在室外或通风良好的地方使用。
  • P312 Call a POISON CENTER or doctor/physician if you feel unwell. 如果你感觉不适,呼叫解毒中心或医生/医师。
  • P302+P352+P312+P362+P364
  • P501 Dispose of contents/container to..… 处理内容物/容器.....
Hazard statements
  • H332 Harmful if inhaled 吸入有害
  • H302 Harmful if swallowed 吞食有害
  • H312 Harmful in contact with skin 皮肤接触有害
  • H302+H312+H332
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
Signal word Warning
Storage condition 0-10 Air & Moisture Sensitive 0-10°C 常温干燥密封储存
Hazard Codes Xn
Safety Statements
  • S36/37 Wear suitable protective clothing and gloves 穿戴适当的防护服和手套;
  • S22 Do not breathe dust 不要吸入粉尘;
Risk Statements
  • R20/21 Harmful by inhalation and in contact with skin 吸入及与皮肤接触有害
  • R20/21/22 Harmful by inhalation, in contact with skin and if swallowed 吸入、皮肤接触和不慎吞咽有害

其他信息

  • 不溶于水,空气中易分解,微溶于甲醇、乙醇、丙酮、乙酸乙酯、氯仿和甲苯,不溶于乙醚和正己烷。

系列性分类


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