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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 847435Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/847435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Hydroxybenzyl AlcoholHCID 125—
Edukt1-(2-Methoxyphenyl)piperazineHCID 1346—
EduktPotassium HydroxideHCID 14797—
EduktLithium BromideHCID 82050—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt4-[[4-(2-Methoxyphenyl)piperazin-1-yl]methyl]phenolHCID 137714956%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05142052
Quelldatensatzuspto-grants-1992_08
ORD IDord-0ebeb5b64dfb451d93a06df6381c57ed
Quellennotizuspto-grants-1992_08