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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280853Erstellt: 24. Oktober 2026

p-Anisoyl chloride → 1-[3-(4-Methoxybenzoylamino)propyl]-4-benzhydrylpiperazine

https://huagongshe.com/de/reaction/280853

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Anisoyl chlorideHCID 7477—
EduktTriethylamineHCID 8471—
Edukt3-(4-Benzhydryl-1-piperazinyl)-1-propanamineHCID 13767778—
LösungsmittelChloroformHCID 6212—
Produkt1-[3-(4-Methoxybenzoylamino)propyl]-4-benzhydrylpiperazineHCID 1336283449,8%

Reaktionsschritte

To a solution of 1-(3-aminopropyl)-4-benzhydrylpiperazine (1.55 g) and triethylamine (0.7 ml) in chloroform (15 ml) was dropwise added p-methoxybenzoyl chloride (0.85 g) at ambient temperature with stirring, which was continued for 20 minutes. The reaction mixture was washed successively with aqueous sodium bicarbonate and water. The organic layer was separated, dried and evaporated in vacuo. The resultant oily product was subjected to column chromatography on silica gel eluting with ethyl acetate. The fractions containing the desired compound were combined and evaporated in vacuo. The residue was crystallized from a mixture of ethyl acetate and hexane to give 1-[3-(4-methoxybenzoylamino)propyl]-4-benzhydrylpiperazine (1.1 g) as white crystals. mp: 126°-128° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04591590
Quelldatensatzuspto-grants-1986_05
ORD IDord-45435e028d2149abb3c42f25079f2be1
Quellennotizuspto-grants-1986_05