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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275488Erstellt: 24. Oktober 2026

Aluminium lithium hydride → 3-Cyclopentyloxy-4-methoxyphenethylamine

https://huagongshe.com/de/reaction/275488

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAluminium lithium hydrideHCID 21226445—
Edukt2-(Cyclopentyloxy)-1-methoxy-4-(2-nitroethenyl)benzeneHCID 54503224—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Cyclopentyloxy-4-methoxyphenethylamineHCID 1127639481%

Reaktionsschritte

To a suspension of lithium aluminum hydride (10.83 g, 28.5 mmol) in ether (250 mL) at 0° C. under an argon atmosphere was added dropwise a solution of 3-cyclopentyloxy-4-methoxy-β-nitrostyrene (15.00 g, 57.0 mmol) in tetrahydrofuran (85 mL). The resulting mixture was allowed to warm to room temperature and stirred overnight. The reaction mixture was cooled to 0° C. and quenched by the successive dropwise addition of water (11 mL), 15% sodium hydroxide (11 mL) and water (33 mL). The mixture was filtered through a pad of Celite™ and the filtrate was washed successively with water, 10% hydrochloric acid and water. The aqueous washes were combined, made basic with saturated aqueous potassium carbonate and extracted three times with ether and twice with methylene chloride. The organic layers were combined and dried (potassium carbonate). Removal of the solvent in vacuo provided the amine (10.80 g, 81%). A portion of the crude amine was purified by flash chromatography, eluting with 1:10:90 water/methanol/chloroform.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05393788
Quelldatensatzuspto-grants-1995_02
ORD IDord-940e1276a546428c810a1f12135aa62c
Quellennotizuspto-grants-1995_02