ChemicalBook--->CAS DataBase List--->1895006-01-5

1895006-01-5

1895006-01-5 Structure

1895006-01-5 Structure
IdentificationBack Directory
[Name]

Mes-Umemoto reagent
[CAS]

1895006-01-5
[Synonyms]

Mes-Umemoto reagent
Mes-Umemoto reagent >=95%
Dimesityl(trifluoromethyl)sulfonium Triflate
dimesityl(trifluoromethyl)sulfonium trifluoromethanesulfonate
[Molecular Formula]

C20H22F6O3S2
[MDL Number]

MFCD31619197
[MOL File]

1895006-01-5.mol
[Molecular Weight]

488.5
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[form ]

powder
[InChI]

InChI=1S/C19H22F3S.CHF3O3S/c1-11-7-13(3)17(14(4)8-11)23(19(20,21)22)18-15(5)9-12(2)10-16(18)6;2-1(3,4)8(5,6)7/h7-10H,1-6H3;(H,5,6,7)/q+1;/p-1
[InChIKey]

HAYTWACXJNSBRL-UHFFFAOYSA-M
[SMILES]

C(F)(F)(F)S([O-])(=O)=O.[S+](C1C(=CC(C)=CC=1C)C)(C1C(=CC(C)=CC=1C)C)C(F)(F)F
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

Under a dual catalytic copper/photoredox manifold, the Mes-Umemoto reagent has been demonstrated by the MacMillan lab to be an excellent reagent for the trifluoromethylation of alkyl halides and aryl halides to yield alkyl-CF3 and aryl-CF3 in high yields. In both cases, these reactions exhibit wide substrate scope with good functional group tolerance. More specifically, a variety of 5-membered and 6-membered heteroaryl halides can be readily converted to the corresponding trifluoromethylheteroarenes under mild conditions. To be use in conjunction with supersilanol (902489) and Ir photocatalyst (902217 or 902225).
[reaction suitability]

reagent type: catalyst
reaction type: Photocatalysis
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