HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → ethyl 5-chloro-3-(trifluoromethyl)-1H-pyrazole-1-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-chloro-3-(trifluoromethyl)-1H-pyrazole | HCID 178506197 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ethyl 5-chloro-3-(trifluoromethyl)-1H-pyrazole-1-acetate | HCID 66016896 | 29.8% |
Reaction Steps
A suspension of 5-chloro-3-trifluoromethyl-1H-pyrazole (2.1 g, 12.3 mmol) (i.e. the product of Example 13, Step C), potassium carbonate (3.6 g, 26 mmol) in N,N-dimethylformamide (20 mL) was treated with ethyl bromoacetate (2.1 mL, 18.8 mmol) and the reaction mixture was stirred at ambient temperature for 12 h. The reaction mixture was diluted with ethyl acetate, washed with water, and dried over MgSO4. The reaction mixture was filtered and concentrated under reduced pressure. The crude product was purified by silica gel chromatography using 0-50% ethyl acetate in hexanes as eluant to give 940 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586611B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-0ed21987bd8b4357ab718ce75638c089 |
| Source note | uspto-grants-2013_11 |