ChemicalBook Product Catalog Chemical Reagents Organic reagents Ionic Liquids 1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride

1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride

Product Name1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride
CAS141556-45-8
MFC21H25ClN2
MW340.89
EINECS
MOL File141556-45-8.mol

Chemical Properties

Melting point	>300 °C (lit.)
Boiling point	499.2°C (rough estimate)
Density	1.0279 (rough estimate)
refractive index	1.5940 (estimate)
storage temp.	under inert gas (nitrogen or Argon) at 2–8 °C
pka	19.40(Temp: 25 °C; Solvent: Dimethyl sulfoxide)
form	Powder
color	Off-white to beige
Water Solubility	Slightly soluble in water.
InChI	InChI=1S/C21H25N2.ClH/c1-14-9-16(3)20(17(4)10-14)22-7-8-23(13-22)21-18(5)11-15(2)12-19(21)6;/h7-13H,1-6H3;1H/q+1;/p-1
InChIKey	OTOSIXGMLYKKOW-UHFFFAOYSA-M
SMILES	N1(C=C[N+](C2C(C)=CC(C)=CC=2C)=C1)C1C(C)=CC(C)=CC=1C.[Cl-]
CAS DataBase Reference	141556-45-8(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36
WGK Germany	3
TSCA	No
HS Code	29332900
Storage Class	11 - Combustible Solids
Hazard Classifications	Eye Irrit. 2 Skin Irrit. 2 STOT SE 3

MSDS

Provider	Language
ACROS	English
SigmaAldrich	English

Usage And Synthesis

Chemical Properties

off-white to beige powder

Uses

1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride is used as a phosphine-free ligand in various metal-catalyzed coupling reactions, often with advantageous results in difficult cases. For use in the Pd-catalyzed cross-coupling of aryl Grignards with aryl chlorides (Kumada reaction). Many examples have been recorded of the use of NHC ligands in the Suzuki coupling reaction, for examples utilizing 1,3-dimesitylimidazol-2-ylidene, in the coupling of arylboronic acids with relatively unreactive aryl chlorides.

Preparation

In a flask, the imine(3 g, 10 mmol) was dissolved in tetrahydrofuran(25 ml), followed by dropwise addition of chloromethyl ethyl ether(1.04 g, 11 mmol). the mixture was stirred under N2 at 40 °C for 18 h, and then ethyl ether(25 ml) was added to separate white solid. The solid was filtered and washed with ethyl ether. Finally, the white solid was dried under vacuum affording 1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride.

1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride

Reactions

Precursor to the nucleophilic carbene that serves as a bulky, electron-rich "phosphine mimic" for metal-catalyzed reactions.
(a) Palladium-catalyzed Suzuki cross-coupling of aryl chlorides.
(b) Palladium-catalyzed Kumada cross-coupling of aryl chlorides.
(c) Ruthenium-carbene catalysts for ring-closing metathesis.
(d) Suzuki coupling of aryltrimethylammonium salts.
(e) Sonogashira coupling of aryl bromides.
Precursor to a nucleophilic carbene that serves as catalyst.
Ligand for arylation of aldehydes.
Ligand for carbene catalyzed intermolecular arylation of C-H bonds.
Catalyst for boron conjugate additions to cyclic and acyclic α,β-unsaturated carbonyls.
Ligand for dehydrogenative cyclocondensation of aldehydes, alkynes, and dialkylsilanes.
Precursor for carbene for conjugate silylation of alpha, beta-unsaturated carbonyls.
Reaction of 1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride

Reaction of 1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride

reaction suitability

reagent type: ligand

Synthesis

N,N'-bis(2,4,6-trimethylphenyl)ethane-1,2-diimine

56222-36-7

3188-13-4

141556-45-8

The general procedure for the synthesis of 1,3-bis(2,4,6-trimethylphenyl)imidazolium chloride from N,N'-bis(2,4,6-trimethylphenyl)ethane-1,2-diimine and chloromethyl ethyl ether is as follows: in a dry flask, N,N'-bis(2,4,6-trimethylphenyl)ethane-1,2-diimine (3 g, 10 mmol) was dissolved in anhydrous tetrahydrofuran ( 25 ml) followed by slow dropwise addition of chloromethyl ethyl ether (1.04 g, 11 mmol). The reaction mixture was stirred at 40 °C for 18 h under nitrogen protection. After completion of the reaction, ether (25 ml) was added to precipitate a white solid. The solid product was collected by filtration and washed with ether and finally dried under vacuum to afford 1,3-bis(2,4,6-trimethylphenyl)imidazole chloride (IMes-HCl) 2.2 g in 65% yield. The structure of the product was confirmed by 1H NMR (CDCl3, 400 MHz) and 13C NMR (CDCl3, 100 MHz): 1H NMR δ 2.15 (s, 12H), 2.33 (s, 6H), 7.00 (s, 4H), 7.70 (s, 2H), 10.73 (s, 1H); 13C NMR δ 17.6, 21.1, 124.8, 129.8, 130.7, 134.1, 139.2, 141.1.

References

[1] Journal of Organic Chemistry, 2008, vol. 73, # 7, p. 2784 - 2791
[2] Tetrahedron Letters, 2012, vol. 53, # 7, p. 815 - 818
[3] Tetrahedron, 2012, vol. 68, # 38, p. 7949 - 7955
[4] Chemical Communications, 2011, vol. 47, # 5, p. 1559 - 1561
[5] Journal of Organometallic Chemistry, 2013, vol. 743, p. 44 - 48

1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride

Chemical Properties

Safety Information

MSDS

Usage And Synthesis

Preparation Products And Raw materials

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