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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16628Erstellt: 24. Oktober 2026

Benzyl Bromide → 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde

https://huagongshe.com/de/reaction/16628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt2-methyl-5-nitro-1H-indole-3-carbaldehydeHCID 609359—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehydeHCID 283825383,2%

Reaktionsschritte

To a solution of 2-methyl-5-nitro-1H-indole-3-carboxaldehyde (500 mg, 2.45 mmol) in DMF (5 ml) was added potassium carbonate (1.0 g, 7.35 mmol) and benzyl bromide (0.44 ml, 3.68 mmol). The mixture was stirred at room temperature for 4 h, diluted with EtOAc, washed with H2O, brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was triturated with Et2O-hexane to yield 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde (Compound 50) as a yellow solid (600 mg, 83%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737173B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-02e4b9ab0bf74da998fa4be994fe94f7
Quellennotizuspto-grants-2010_06