HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 5-chloro-2-(2-trifluoromethylphenyl)pentanimidoate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 5-Chloro-2-(2-trifluoromethylphenyl)pentanenitrile | HCID 66839598 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Ethyl 5-chloro-2-(2-trifluoromethylphenyl)pentanimidoate hydrochloride | HCID 46854983 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
5-Chloro-2-(2-trifluoromethylphenyl)pentanenitrile (2.0 g, 7.64 mmol) was dissolved in ethanol (5.36 mL, 91.72 mmol) at room temperature under nitrogen atmosphere. Then, the solution was cooled to 0° C. Acetyl chloride (4.34 mL, 61.14 mmol) was added dropwise to the solution, and the reaction mixture was stirred at room temperature for 67 hours. The reaction mixture was cooled to 10° C. Traces of seed crystal of the title compound which was obtained by the method similar to this step and tert-butylmethylether (hereinafter referred to as “MTBE”) (40 mL) were added to the reaction mixture and the reaction mixture was stirred. The solid was collected by filtration, washed with MTBE to obtain the title compound (2.14 g, 81.6% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935815B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-6a8f3885b2c44ce894efbc4ec6172ff1 |
| Source note | uspto-grants-2011_05 |