HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Ethyl 3-oxo-3-(2,4,5-trifluoro-3-methylphenyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 14052571 | HCID 14052571 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-oxo-3-(2,4,5-trifluoro-3-methylphenyl)propanoate | HCID 14052572 | 8% |
Reaction Steps
A mixture of diethyl 2-(2,4,5-trifluoro-3-methylbenzoyl)malonate (8.10 g) and p-toluenesulfonic acid (9.6 mg) in water (9.6 ml) was refluxed for 3 hours with stirring vigorously. After cooling, the reacting mixture was extracted with dichloromethane. The organic layer was washed with 7% aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resulting residue was allowed to stand in a refrigerator for 2 days, the resulting precipitate was collected by filtration and recrystallized from n-hexane to give the title compound (0.51 g) as colorless prisms, mp 38°-39° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04894458 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-f74b2889e99c4b4f8541a76caf6f5a2f |
| Source note | uspto-grants-1990_01 |