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 suspension of 45.3 g of diethyl (2,4,5-trifluoro-3-methyl-6-nitrobenzoyl)malonate and 30 mg of p-toluenesulfonic acid in 120 ml of water was heated at reflux for 50 minutes. After cooling, the reaction mixture was extracted with diethyl ether. The combined organic extracts were washed with brine, dried and evaporated to give 34.2 g of the desired compound as brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05547962 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-5eb8e74a998c49aa973b54735318eb10 |
| Source note | uspto-grants-1996_08 |