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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2215780Erstellt: 24. Oktober 2026

Methyl iodide → 1,5-Dimethyl-7-bromoindole

https://huagongshe.com/de/reaction/2215780

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt7-Bromo-5-methyl-1H-indoleHCID 3403330—
LösungsmittelDimethylformamideHCID 6228—
Produkt1,5-Dimethyl-7-bromoindoleHCID 2194996296%

Reaktionsschritte

To a suspension of sodium hydride (60%, 0.91 g, 22.9 mmol) in DMF (70 mL) was added a solution of 5-methyl-7-bromoindole (4.0 g, 19.05 mmol) in DMF (10 mL). The mixture was stirred at room temperature for 1 h, and then methyl iodide (1.78 mL, 28.6 mmol) was added with cooling in an ice-water-bath. The reaction mixture was allowed to warm to room temperature and stirred overnight. The reaction was quenched with water and extracted with ethyl acetate. The extract was washed with water and brine, dried (sodium sulfate) and concentrated to give a crude product (4.1 g, 96%), which was used without further purification. 1H NMR (400 MHz, CDCl3) δ 2.38 (s, 3H), 4.12 (s, 3H), 6.36 (d, J=3.12 Hz, 1H), 6.95 (d, J=3.13 Hz, 1H), 7.18 (d, J=1.56 Hz, 1H), 7.31 (dd, J1=0.79 Hz, J2=1.56 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07109229B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-12bc21d35cd446ed8b153ecd0cccc676
Quellennotizuspto-grants-2006_09