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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1614633Erstellt: 26. Oktober 2026

1-Butanol → N,alpha-Bis(4-Fluorophenyl)-1-[2(2-naphthalenyloxy)ethyl]-4-piperidinemethanamine hydrochloride

https://huagongshe.com/reaction/1614633

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-ButanolHCID 263—
EduktHydrochloric AcidHCID 313—
EduktSodium IodideHCID 5238—
EduktPotassium CarbonateHCID 11430—
Edukt1-(2-Bromoethoxy)naphthaleneHCID 11075906—
EduktN,alpha-bis(4-fluorophenyl)-4-piperidinemethanamineHCID 19771957—
LösungsmittelDiethyl ether methanolHCID 21864698—
ProduktN,alpha-Bis(4-Fluorophenyl)-1-[2(2-naphthalenyloxy)ethyl]-4-piperidinemethanamine hydrochlorideHCID 1977200936,3%

Reaktionsschritte

A mixture of N,α-bis(4-fluorophenyl)-4-piperidinemethanamine (3.42 g, 0.0113 mol), 2-bromoethyl naphthyl ether (2.83 g, 0.0113 mol), and potassium carbonate (3.46 g, 0.025 mol) was heated at reflux 16 h in 350 mL of 1-butanol containing sodium iodide (0.2 g). The reaction was concentrated to dryness, and the residue partitioned between chloroform and water. The chloroform layer was extracted with 5% sodium hydroxide. The organic layer was dried (Na2SO4) and filtered. The chloroform was removed by rotary evaporator to give a brown residue. This material was subjected to flash chromatography on silica gel. Elution was accomplished using methylene chloride, 1% methanol-methylene chloride, and 2% methanol-methylene chloride. Fractions of similar purity were combined and solvents removed. A brown residue was obtained and converted to the HCl salt in methanol-diethyl ether and placed in the freezer. A white solid was isolated and dried 16 h at 78° C. This process provided 2.24 g (36.3%) of white crystalline product mp 226°-230° C. (dec.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05198449
Quelldatensatzuspto-grants-1993_03
ORD IDord-2dae01b11616487984150efc5dfe29fc
Quellennotizuspto-grants-1993_03