HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-1,1,1-trifluoro-2-propanone → 1-Methyl-2-(2-naphthyl)-5-(trifluoromethyl)pyrrole-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-1,1,1-trifluoro-2-propanone | HCID 79008 | — |
| Reactant | beta-(Methylamino)-2-naphthaleneacrylonitrile | HCID 67791408 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Methyl-2-(2-naphthyl)-5-(trifluoromethyl)pyrrole-3-carbonitrile | HCID 19890304 | — |
Reaction Steps
A solution of β-(methylamino)-2-naphthaleneacrylonitrile (2.5 g, 0.012 mol) in toluene and acetic acid is treated dropwise with 3-bromo-1,1,1-trifluoro-2-propanone (2.3 g, 0.012 mol) at room temperature, heated at reflux temperature for 6 hours, cooled and diluted with ethyl acetate. The organic phase is washed sequentially with water and 5N NaOH, dried (Na2SO4) and concentrated in vacuo to give a brown oil residue. The residue is flash chromatographed (silica gel, hexanes/ethyl acetate, 80/20) to give the title compound as a yellow solid, mp 134° C., identified by mass spectral, IR and NMR analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05128485 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-3a3b6d1aa39047efabc8e380c887c679 |
| Source note | uspto-grants-1992_07 |