Reaktion #74860

ord-b4933e6ff4514b2a8f47b2d1faa81725

Reaktionsgleichung

COS(=O)(=O)C(F)(F)F
methyl trifluoromethanesulfonate
O=c1cccc[nH]1
pyridinone
Cn1cc(-c2ccccc2)c(=O)c(-c2cccc(Br)c2)c1
3-(3-bromophenyl)-1-methyl-5-phenyl-4(1H)-pyridinone
CC(C)=O
2-propanone
COc1c(-c2ccccc2)c[n+](C)cc1-c1cccc(Br)c1.O=S(=O)([O-])C(F)(F)F
3-(3-bromophenyl)-4-methoxy-1-methyl-5-phenylpyridinium trifluoromethanesulfonate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe volatile portions were then evaporated under vacuum

Vorschrift

A 10 g. portion of 3-(3-bromophenyl)-1-methyl-5-phenyl-4(1H)-pyridinone was made from 22 g. of the corresponding 2-propanone as described in Example 1. A 3.4 g. portion of the intermediate pyridinone was dissolved in chloroform and 1.8 g. of methyl trifluoromethanesulfonate was added. The reaction mixture was allowed to stand overnight, and the volatile portions were then evaporated under vacuum. The residue was identified as 3-(3-bromophenyl)-4-methoxy-1-methyl-5-phenylpyridinium trifluoromethanesulfonate, molecular weight 339 by mass spectroscopy.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04174209uspto-grants-1979_11