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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 565686Erstellt: 26. Oktober 2026

Triethylamine → 2,3-Dihydro-2,4,6,7-tetramethyl-2-[[4-(2-phenylethyl)-1-piperidinyl]methyl]-5-benzofuranamine

https://huagongshe.com/reaction/565686

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-(2-Phenylethyl)piperidineHCID 4341895—
Edukt2-Bromomethyl-2,3-dihydro-2,4,6,7-tetramethyl-5-benzofuranamineHCID 10850590—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt2,3-Dihydro-2,4,6,7-tetramethyl-2-[[4-(2-phenylethyl)-1-piperidinyl]methyl]-5-benzofuranamineHCID 1548587742,5%

Reaktionsbedingungen

Temperatur180 °C

Reaktionsschritte

In an autoclave, a mixture of 2-bromomethyl-2,3-dihydro-2,4,6,7-tetramethyl-5-benzofuranamine (1.5 g), 4-(2-phenylethyl)piperidine (2.0 g), and triethylamine (5.3 g) was stirred under argon gas at 180° C. for 15 hours. After cooling, the reaction mixture was diluted with saturated aqueous NaHCO3 and extracted with ethyl acetate. The extract was washed with saturated aqueous NaCl and dried over MgSO4 and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1:1) and recrystallized from diisopropyl ether to provide 0.88 g of the title compound. Yield 42%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06172085B2
Quelldatensatzuspto-grants-2001_01
ORD IDord-48191aeed5bb4d0e9fa03d8a3961a655
Quellennotizuspto-grants-2001_01