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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 620042Erstellt: 26. Oktober 2026

Potassium Carbonate → 1-(4-Hydroxyphenyl)-4-(benzoxazol-2-yl)piperazine

https://huagongshe.com/reaction/620042

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2-ChlorobenzoxazoleHCID 11986—
Eduktp-(1-Piperazinyl)phenol dihydrobromideHCID 2723591—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(4-Hydroxyphenyl)-4-(benzoxazol-2-yl)piperazineHCID 1407416897,1%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A mixture of 5.11 g (15 mmol) of 1-(4-hydroxyphenyl)piperazine dihydrobromide, 2.46 g (16 mmol) of 2-chlorobenzoxazole and 2.18 g (15.8 mmol) of powdered K2CO3 in 55 ml of absolute N,N-dimethylformamide was warmed to 85° C., and 345 mg of powdered K2CO3 were added with stirring under a nitrogen atmosphere in each case after 10 minutes, after a further 25 minutes and after a further 60 minutes (total addition of 1.035 g (7.5 mmol) of K2CO3). The mixture was stirred for a further 3 hours at 85° C., the DMF was substantially removed by distillation in an oil-pump vacuum in a rotary evaporator, the crystalline residue was mixed with 50 ml of water, and this mixture was shaken for 15 minutes. The mixture was then filtered under suction and the filter residue was washed with water and dried in vacuo. 4.30 g (97% of theory) of pure 1-(4-hydroxyphenyl)-4-(benzoxazol-2-yl)piperazine, melting point 161°-3° C., were obtained,

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04818758
Quelldatensatzuspto-grants-1989_04
ORD IDord-3f4b8fdb47f94dfdab03d170978fb3fe
Quellennotizuspto-grants-1989_04