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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1886667Erstellt: 26. Oktober 2026

1-Benzylpiperazine → 1-[3-(4-Fluorophenoxy)-1-azetidinylcarbonyl]-4-(phenylmethyl)piperazine

https://huagongshe.com/reaction/1886667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BenzylpiperazineHCID 75994—
Edukt3-(4-Fluorophenoxy)-1-azetidinecarbonyl chlorideHCID 15053367—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-[3-(4-Fluorophenoxy)-1-azetidinylcarbonyl]-4-(phenylmethyl)piperazineHCID 15053405108,3%

Reaktionsschritte

A stirred solution of 6.9 g (0.03 mole) of 3-(4-fluorophenoxy)-1-azetidinecarbonyl chloride in 60 ml of methylene chloride was treated with 10.8 g (0.06 mole) of 1-benzylpiperazine, added dropwise. After stirring for 18 hr, the reaction mixture was diluted with 200 ml of water and stirred for an additional 1 hr. The methylene chloride portion was separated and the aqueous portion was extracted with 2×25 ml of methylene chloride. The methylene chloride portions were combined, dried and concentrated in vacuo, yielding 12 g of oil residue. This oil solidified when triturated with ligroin and was recrystallized from benzene/ligroin to yield 10.1 (91%) of tan crystals. A 500 mg portion was recrystallized from benzene/ligroin to yield 250 mg of fine white crystals, m.p. 109°-111° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05151418
Quelldatensatzuspto-grants-1992_09
ORD IDord-e85d4c3b1910426fbbe4be17e1b79c9a
Quellennotizuspto-grants-1992_09