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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847435Generated: October 27, 2026

4-Hydroxybenzyl Alcohol → 4-[[4-(2-Methoxyphenyl)piperazin-1-yl]methyl]phenol

https://huagongshe.com/reaction/847435

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantPotassium HydroxideHCID 14797—
ReactantLithium BromideHCID 82050—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-[[4-(2-Methoxyphenyl)piperazin-1-yl]methyl]phenolHCID 137714956%

Reaction Steps

4-Hydroxyphenyl methanol (124 g, 1 mole) and 192 g (1 mole) of 1-(2-methoxyphenyl)piperazine, together with 56 g (1 mole) of potassium hydroxide and 8.7 g (0.1 mole) of lithium bromide and 32.2 g (0.1 mole) of Aliquat 366 were dissolved in a mixture of 1 liter of toluene and 1 liter of water. The reaction mixture was refluxed for 24 hours, and then allowed to cool to room temperature. The organic layer was decanted and extracted twice with 500 ml of a 10% sodium hydroxide solution. The basic aqueous liquor was treated with ammonium acetate to provoke precipitation of the desired product. After filtration and drying under vacuum overnight at 50° C., 167 g (0.56 mole, 56% yield) of the title product was obtained as small white leaflets melting at 172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05142052
Source datasetuspto-grants-1992_08
ORD IDord-0ebeb5b64dfb451d93a06df6381c57ed
Source noteuspto-grants-1992_08