HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 11431005, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Phenylethanol | HCID 6054 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | [4-(6-Chloropyridazin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)methanone | HCID 86024941 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11431005 | HCID 11431005 | 62.9% |
Reaction Steps
A mixture of [4-(6-chloropyridazin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)-methanone (0.075 g, 0.202 mmol), 2-phenylethanol (0.025 g, 0.202 mmol) and sodium hydride (0.010 g) in 5 mL of toluene was stirred at room temperature for 1 hour, and then refluxed overnight. The reaction mixture was cooled to room temperature, added 20 mL of water, and then extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous sodium sulphate, concentrated in vacuo. The residue was purified by column chromatography to yield the title compound as a white solid (58 mg, 62.9%). 1H NMR (400 MHz, CDCl3) δ 7.73, 7.61-7.64, 7.53-7.56, 7.36, 7.22-7.30, 7.20-7.24, 7.02, 6.86, 4.64, 3.91-3.98, 3.57, 3.48-3.52, 3.32, 3.11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514436B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-c02a5202a5a5445c94edb7ea5653a9c6 |
| Source note | uspto-grants-2009_04 |