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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108371Generated: October 30, 2026

Water → HCID 11431005, compound

https://huagongshe.com/reaction/2108371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-PhenylethanolHCID 6054—
ReactantSodium hydrideHCID 24758—
Reactant[4-(6-Chloropyridazin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)methanoneHCID 86024941—
SolventTolueneHCID 1140—
ProductHCID 11431005HCID 1143100562.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514436B2
Source datasetuspto-grants-2009_04
ORD IDord-c02a5202a5a5445c94edb7ea5653a9c6
Source noteuspto-grants-2009_04