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N-[3-ALPHA,ALPHA,ALPHA-TRIFLUOROMETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLYL)]-N-METHYL-N-PHENYLAMINE

Compound with spectra: 3 NMR

N-[3-ALPHA,ALPHA,ALPHA-TRIFLUOROMETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLYL)]-N-METHYL-N-PHENYLAMINE
SpectraBase Compound ID L2XIJHsRFv0
InChI InChI=1S/C20H23BF3NO2/c1-18(2)19(3,4)27-21(26-18)15-11-14(20(22,23)24)12-17(13-15)25(5)16-9-7-6-8-10-16/h6-13H,1-5H3
InChIKey IMKOTMQLZKTFBS-UHFFFAOYSA-N
Mol Weight 377.2 g/mol
Molecular Formula C20H23BF3NO2
Exact Mass 377.177394 g/mol

View Spectrum of N-[3-ALPHA,ALPHA,ALPHA-TRIFLUOROMETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLYL)]-N-METHYL-N-PHENYLAMINE

11B NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6

View Spectrum of N-[3-ALPHA,ALPHA,ALPHA-TRIFLUOROMETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLYL)]-N-METHYL-N-PHENYLAMINE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6

View Spectrum of N-[3-ALPHA,ALPHA,ALPHA-TRIFLUOROMETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLYL)]-N-METHYL-N-PHENYLAMINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
METHYL-3-AMINOPHENYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLYL)-BENZOATE
4,4,5,5-tetramethyl-2-(2-(trifluoromethoxy)-5-(trifluoromethyl)phenyl)-1,3,2-dioxaborolane
[4-[3-(hexoxymethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]phenyl]-trimethyl-silane
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-chromen-2- one
Methyl 4-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
[2.2]-Paracyclophanyl-4-boronic acid - Pinacol ester
2-(4-methoxy-[1,1'-biphenyl]-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Flufenamic acid 2ME
2-Chloro-3,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazole
Title Journal or Book Year
One-Pot Borylation/Amination Reactions:  Syntheses of Arylamine Boronate Esters from Halogenated Arenes Organic Letters 2006
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