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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324639Erstellt: 25. Oktober 2026

Ethanol, reaction products with ammonia, distn. residues → 2-(1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-yl)ethylamine hydrobromide

https://huagongshe.com/reaction/324639

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanol, reaction products with ammonia, distn. residuesHCID 22020343—
Edukt(E)-(4-bromo-1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-ylidene)acetonitrileHCID 68423466—
EduktHCID 178418361HCID 178418361—
KatalysatorNickelHCID 935—
LösungsmittelEthanolHCID 702—
Produkt2-(1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-yl)ethylamine hydrobromideHCID 2200477893%

Reaktionsschritte

Raney nickel (0.4 g, W2) and 4M ammonia/ethanol solution (10 ml) were added to an ethanol (30 ml) suspension of (E)-(4-bromo-1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-ylidene)acetonitrile (0.44 g, 1.59 mmols) and stirred in a hydrogen atmosphere (at from 4 to 5 atmospheres) at room temperature for 5 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethanol (50 ml), and 5% palladium-carbon (1 g, containing 50% water) was added thereto and stirred in a hydrogen atmosphere (at ordinary pressure) at room temperature for 4 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure to obtain 0.42 g (yield: 93%) of the target compound. This was amorphous.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218429B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-dc2d90b58c8d4eb1bf6b0cfdc5333fd3
Quellennotizuspto-grants-2001_04