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208523

Sigma-Aldrich

Ruthenium(III) chloride

Ru content 45-55%

Synonym(s):

Ruthenium trichloride

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About This Item

Linear Formula:
RuCl3
CAS Number:
10049-08-8
Molecular Weight:
207.43
EC Number:
233-167-5
MDL number:
MFCD00011208
UNSPSC Code:
12161600
PubChem Substance ID:
24852520
NACRES:
NA.22

form

solid

reaction suitability

core: ruthenium
reagent type: catalyst
reaction type: Atom Transfer Radical Polymerization (ATRP)

density

3.11 g/mL at 25 °C (lit.)

SMILES string

Cl[Ru](Cl)Cl

InChI

1S/3ClH.Ru/h3*1H;/q;;;+3/p-3

InChI key

YBCAZPLXEGKKFM-UHFFFAOYSA-K

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General description

Ruthenium(III) chloride is a chemical compound, that can be used as a mild Lewis acid catalyst for the acetalization of aldehydes, acetalization of alcohols, and conversion of ketoximes to amides. Additionally, it can also be used as a precursor to synthesize Ru nanoparticles.

Application

Ruthenium(III) chloride is used as a catalyst:

  • In the synthesis of β‐amino alcohols by nucleophilic opening of epoxides with anilines.
  • In the acetylation of varies of phenols, alcohols, thiols, and amines under mild conditions.
  • In the synthesis of α‐aminonitriles by mixing aldehydes, amines, and trimethylsilyl cyanides.

Other Notes

insoluble form

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Shū Kobayashi et al.
Organic letters, 4(8), 1319-1322 (2002-04-13)
Several transition metal salts were found to catalyze aza-Michael reactions of enones with carbamates efficiently. The catalytic activity was strongly dependent on the nature of the metal salts. While conventional Lewis acids such as BF(3).OEt(2), AlCl(3), or TiCl(4) showed lower
Hitoshi Harada et al.
The Journal of organic chemistry, 73(17), 6772-6779 (2008-08-07)
Highly enantioselective catalytic intramolecular ortho-alkylation of aromatic imines containing alkenyl groups tethered at the meta position relative to the imine directing group has been achieved using [RhCl(coe)2]2 and chiral phosphoramidite ligands. Cyclization of substrates containing 1,1- and 1,2-disubstituted as well
Halloysite nanotube supported Ru nanocatalysts synthesized by the inclusion of preformed Ru nanoparticles for preferential oxidation of CO in H2-rich atmosphere
Wang L, et al
The Journal of Physical Chemistry C, 117(8), 4141-4151 (2013)
Ruthenium (III) chloride catalyzed acylation of alcohols, phenols, thiols, and amines
De SK
Tetrahedron Letters, 45(14), 2919-2922 (2004)
Takaya Terashima et al.
Macromolecular rapid communications, 33(9), 833-841 (2012-04-25)
Multifunctional microgel-core star polymers with ruthenium catalysts are designed as catalyst-bearing nanoreactors to improve activity, controllability, and functionality tolerance in living radical polymerization. Multifunctional ligands are efficiently incorporated into the core of star polymers by sequential tandem procedures: 1) ruthenium-catalyzed
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