HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Ethyl (2,4,5-trifluoro-3-methyl-6-nitrobenzoyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Diethyl (2,4,5-trifluoro-3-methyl-6-nitrobenzoyl)malonate | HCID 11793970 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl (2,4,5-trifluoro-3-methyl-6-nitrobenzoyl)acetate | HCID 10590663 | 93.3% |
Reaction Steps
A mixture of 45.3 g of diethyl (2,4,5-trifluoro-3-methyl-6-nitrobenzoyl)malonate, 30 mg of p-toluenesulfonic acid, and 120 ml of water was heated under reflux for 50 minutes. After cooling, the reaction mixture was extracted with diethyl ether, and the extract was washed with brine, and then dried and concentrated to give 34.2 g of brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859026 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-8863449dc13f40c1b1d081be03754d1b |
| Source note | uspto-grants-1999_01 |