HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-[3-Chloro-5-(trifluoromethyl)-2-pyridyl]-1-(2-nitrophenyl)-2-propen-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Nitro-1-phenylethanone | HCID 94833 | — |
| Reactant | 3-Chloro-5-(trifluoromethyl)picolinaldehyde | HCID 22018790 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[3-Chloro-5-(trifluoromethyl)-2-pyridyl]-1-(2-nitrophenyl)-2-propen-1-one | HCID 68616401 | — |
Reaction Steps
Sodium hydroxide (0.55 g) was dissolved in water (5 ml) and the resulting solution was diluted with ethanol (3 ml). 2-Nitroacetophenone (1.8 g) was added at 20° C., and the solution was stirred for 5 minutes. 3-Chloro-5-(trifluoromethyl)pyridine-2-carboxaldehyde (2.25 g) was added and stirring was continued for 16 hours. The solution was acidified with acetic acid, the organic layer separated, dried over magnesium sulfate, filtered and evaporated to give a brown oil. Silica gel column chromatography, followed by recrystallisation (petrol) afforded the title compound, 88-9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06939882B1 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-3939677ceb034ef6ba89aa773beedaf9 |
| Source note | uspto-grants-2005_09 |