HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 3-(3-Bromophenyl)-4-methoxy-1-methyl-5-phenylpyridinium trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 2-Pyridone | HCID 8871 | — |
| Reactant | Methyl triflate | HCID 9526 | — |
| Reactant | 3-(3-Bromophenyl)-1-methyl-5-phenylpyridin-4(1H)-one | HCID 12879275 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(3-Bromophenyl)-4-methoxy-1-methyl-5-phenylpyridinium trifluoromethanesulfonate | HCID 23345772 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174209 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-b4933e6ff4514b2a8f47b2d1faa81725 |
| Source note | uspto-grants-1979_11 |