HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 14071800, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Diethyl (2,3-dichloro-4,5-difluorobenzoyl)propanedioate | HCID 14071801 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14071800 | HCID 14071800 | 54.3% |
Reaction Steps
To an emulsion of diethyl 2-(2,3-dichloro-4,5-difluorobenzoyl)malonate (9.71 g) in water (11.2 ml) was added p-toluenesulfonic acid (11.2 mg) and refluxed for 3 hours with stirring vigorously. After cooling, the reaction mixture was extracted with dichloromethane. The organic layer was washed with 7% aqueous sodium carbonate solution and then with water successively, dried over anhydrous sodium sulfate and concentrated. The residue was recrystallized from n-hexane to give the title compound (4.24 g) as powdery crystals. mp 52°-53° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788320 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-af1a0b5108454488a84e0a2c09cff29b |
| Source note | uspto-grants-1988_11 |