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3,3-dichloro-4-(chloromethyl)-2-pyrrolidone

Compound with spectra: 1 NMR, and 2 MS (GC)

3,3-dichloro-4-(chloromethyl)-2-pyrrolidone
SpectraBase Compound ID G8Cq4w6h4Lo
InChI InChI=1S/C5H6Cl3NO/c6-1-3-2-9-4(10)5(3,7)8/h3H,1-2H2,(H,9,10)
InChIKey ZTRACGCGNSQXDR-UHFFFAOYSA-N
Mol Weight 202.47 g/mol
Molecular Formula C5H6Cl3NO
Exact Mass 200.951497 g/mol

View Spectrum of 3,3-dichloro-4-(chloromethyl)-2-pyrrolidone

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QF-10-744-15

View Spectrum of 3,3-dichloro-4-(chloromethyl)-2-pyrrolidone

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum U1-2014-6744-5c

View Spectrum of 3,3-dichloro-4-(chloromethyl)-2-pyrrolidone

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 3,3-Bis(chloranyl)-4-(chloromethyl)pyrrolidin-2-one
3,3-dichlorohexahydro-2(1H)-azocinone
N-tert-butyl-2,2-bis(chloranyl)-3,3-dimethyl-butanamide
N-Propyl-2-bromo-2-chloro-3-methylbutanamide
3-Hydroxy-3,4-dimethyl-2-pyrrolidinone
N-[2-(2,2-dichlorocyclopropyl)ethyl]-2,2-dimethylpropionamide
3-chloroazacycloundecane-2-one
3-CHLOROAZACYCLODODECAN-2-ONE
3-CHLOROOCTAHYDRO-2(1H)-AZECINONE
1-(TRICHLOROACETYL)-4-PIPECOLINE
2,2-Dichloro-3-n-butylcyclobutanone
Title Journal or Book Year
Transition metal catalyzed radical cyclization: new preparative route to .gamma.-lactams from allylic alcohols via the [3.3]-sigmatropic rearrangement of allylic trichloroacetimidates and the subsequent ruthenium-catalyzed cyclization of N-allyltrichloroacetamides The Journal of Organic Chemistry 1992

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