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(+/-)-N-TERT.-BUTYL-2-HYDROXY-2-(4-TRIFLUOROMETHYLPHENYL)-ACETAMIDE

Compound with spectra: 2 NMR

(+/-)-N-TERT.-BUTYL-2-HYDROXY-2-(4-TRIFLUOROMETHYLPHENYL)-ACETAMIDE
SpectraBase Compound ID DYsa1PWByWu
InChI InChI=1S/C13H16F3NO2/c1-12(2,3)17-11(19)10(18)8-4-6-9(7-5-8)13(14,15)16/h4-7,10,18H,1-3H3,(H,17,19)
InChIKey CRALYUBZAAUTGQ-UHFFFAOYSA-N
Mol Weight 275.27 g/mol
Molecular Formula C13H16F3NO2
Exact Mass 275.113313 g/mol

View Spectrum of (+/-)-N-TERT.-BUTYL-2-HYDROXY-2-(4-TRIFLUOROMETHYLPHENYL)-ACETAMIDE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (+/-)-N-TERT.-BUTYL-2-HYDROXY-2-(4-TRIFLUOROMETHYLPHENYL)-ACETAMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
[2-(4-Bromophenyl)-2-hydroxyacetylamino]acetic acid, ethyl ester
(R)-N-([S]-1-Hydroxymethyl-2-methyl-propyl)-mandelamide
[p-(Trifluoromethyl)phenyl]cyclohexyl-methanol
N-mandeloyl-p-toluidine
rac-1-[4-(Trifluoromethyl)phenyl]ethyl decanoate
N,N-Dibutyl-2-hydroxy-2-phenylacetamide
1,1,1-trifluoro-2-(4-(trifluoromethyl)phenyl)propan-2-ol
2-[4-(Trifluoromethyl)phenyl]butanohydroximoyl chloride
2-bromo-2-phenyl-N-(1,1,3,3-tetramethylbutyl)acetamide
N-Benzyl-2-(p-tolyl)propanamide
Title Journal or Book Year
The First Catalytic, Asymmetric α-Additions of Isocyanides. Lewis-Base-Catalyzed, Enantioselective Passerini-Type Reactions Journal of the American Chemical Society 2003
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