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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276880Erstellt: 24. Oktober 2026

1,4-Dibromobutane → 2a-(4-Bromobutyl)-2a,3,4,5-tetrahydrobenz[cd]indole-2(1H)-one

https://huagongshe.com/de/reaction/276880

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DibromobutaneHCID 8056—
EduktSodium hydrideHCID 24758—
Edukt2a,3,4,5-Tetrahydrobenzo[cd]indol-2(1H)-oneHCID 599375—
LösungsmittelDimethylformamideHCID 6228—
Produkt2a-(4-Bromobutyl)-2a,3,4,5-tetrahydrobenz[cd]indole-2(1H)-oneHCID 1059089434,1%

Reaktionsschritte

2a, 3,4,5-Tetrahydrobenz [cd]indole-2(1H) -one (3.0 g, 17 mmol) was dissolved in anhydrous N,N-dimethylformamide (120 ml). Thereto was added an oily sodium hydride (760 mg, 19 mmol), and the resulting solution was stirred at a room temperature for 1 hour. The reaction solution was mixed with 1,4-dibromobutane (6.3 ml, 52 mmol) and again stirred for 17 hours. The solvent was evaporated under a reduced pressure, and the thus obtained residue was mixed with ethyl acetate, water and hydrochloric acid (1 N). The reaction product was extracted with ethyl acetate, washed with saturated brine and dried with anhydrous sodium sulfate. Then the compound obtained by the evaporation of the solvent under a reduced pressure was separated and purified by a silica gel column chromatography to obtain 1.8 g of the title compound (5.8 mmol, 33% in yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06355642B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-47990322cb844c318103aa69840dda39
Quellennotizuspto-grants-2002_03