HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Ethyl (2-bromo-4,5-difluorobenzoyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Diethyl (2-bromo-4,5-difluorobenzoyl)malonate | HCID 14347789 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl (2-bromo-4,5-difluorobenzoyl)acetate | HCID 13912599 | 84.9% |
Reaction Steps
To a solution of diethyl (2-bromo-4,5-difluorobenzoyl)malonate (75.6 g) in water (100 ml) is added p-toluenesulfonic acid (0.3 g), and the mixture is refluxed for 3 hours. After cooling, the reaction mixture is extracted with dichloromethane. The dichloromethane layer is washed with saturated aqueous sodium chloride solution and dried over magnesium sulfate. After distilling off the solvent under reduced pressure, the residue is distilled to give ethyl (2-bromo-4,5-difluorobenzoyl)acetate (52.0 g), b.p. 105°-115° C. (0.15 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04786649 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-82cc8cba5b594f5c9d9e360d2b1958ea |
| Source note | uspto-grants-1988_11 |