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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584208Generated: November 1, 2026

Formaldehyde → (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-(4-hydroxy-2-butynyl)piperazine

https://huagongshe.com/reaction/584208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPotassium IodideHCID 4875—
ReactantPropargyl alcoholHCID 7859—
ReactantSodium BicarbonateHCID 516892—
Reactant(2R)-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)piperazineHCID 54478438—
CatalystCopper sulfate pentahydrateHCID 24463—
Solvent1,4-DioxaneHCID 31275—
Product(2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-(4-hydroxy-2-butynyl)piperazineHCID 86588520—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 37% aqueous formaldehyde (0.21 g), (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)piperazine (0.75.g), propargyl alcohol (0.11 ml), copper(II) sulfate pentahydrate (1.3 mg) and potassium iodide (2.8 mg) in 1,4-dioxane was stirred at 100° C. for 2 hours. After being cooled to room temperature, the mixture was made basic with aqueous saturated sodium hydrogen carbonate solution. The resulting mixture was filtered and the filtrate was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixed solvent of n-hexane and ethyl acetate (4:1). The fractions containing the objective compound was collected and evaporated under reduced pressure to give (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-(4-hydroxy-2-butynyl)piperazine (0.78 g) as a syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924278B2
Source datasetuspto-grants-2005_08
ORD IDord-53559e9e13004f18822b7469771586da
Source noteuspto-grants-2005_08