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Merck
CN

425702

Praseodymium(III) trifluoromethanesulfonate

98%

Synonym(s):

Praseodymium(III) triflate

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About This Item

Linear Formula:
(CF3SO3)3Pr
CAS Number:
52093-27-3
Molecular Weight:
588.12
NACRES:
NA.22
PubChem Substance ID:
24866660
UNSPSC Code:
12352300
MDL number:
MFCD00192417

Key Documents

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InChI

1S/3CHF3O3S.Pr/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3

SMILES string

[Pr+3].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F

InChI key

ROUBZIWQWFQCHU-UHFFFAOYSA-K

assay

98%

reaction suitability

core: praseodymium, reagent type: catalyst
reaction type: Ring-Opening Polymerization

General description

Praseodymium (III) trifluoromethanesulfonate (Praseodymium(III) triflate) is a water-tolerant Lewis acid. It is an efficient catalyst employed for the synthesis of α-aminonitrile, via condensation of aldehydes, amines and trimethylsilyl cyanide.

Application

Catalyst for:
  • Asymmetric α-amination reactions
  • Polymerization reactions
  • Regioselective reductive ring opening reactions
  • Intermolecular hydroamination reactions
  • Paal-Knorr condensation
  • Friedel-Crafts alkenylation
  • Friedel-Crafts acylation
  • Biginelli reactions
Praseodymium(III) trifluoromethanesulfonate (Praseodymium(III) triflate) was employed as catalyst for the aqueous aza-Diels-Alder reactions of aldehydes and dienes. It was also used as catalyst for the Aldol reaction of silyl enol ethers with aldehydes.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBW0828V
MKBD1511
10316KI
14913EG

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Yu L, Chen D, Wang PG
Tetrahedron Letters, 37, 2169-2169 (1996)
Praseodymium Trifluoromethylsulfonate as an Efficient and Recyclable Catalyst for the Synthesis of a-Aminonitriles.
De SK and Gibbs RA.
Synthetic Communications, 35(7), 961-966 (2005)
The Journal of Organic Chemistry, 59, 3590-3590 (1994)

Articles

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