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HRID 913964Erstellt: 26. Oktober 2026

Dimethylformamide → 7-bromo-5-chloro-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/913964

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPhosphorus oxychlorideHCID 24813—
Edukt7-bromo-5-chloro-1H-indoleHCID 24729504—
Produkt7-bromo-5-chloro-1H-indole-3-carbaldehydeHCID 5754611382%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Phosphorus oxychloride (3.11 mL, 33.4 mmol) was added dropwise to a 0° C sample of DMF (30 mL). The reaction was stirred 30 min at 0° C., then 7-bromo-5-chloro-1H-indole (7.0 g, 30.4 mmol) in DMF (5 mL)was added and the reaction was warmed to ambient temperature and stirred 20 hours. Ice water (300 mL) was added, and the resulting thick solid was filtered. The product was detected by TLC in both filtrate and cake. Cake and filtrate were combined, and sodium hydroxide (10N) was added until most solids disappeared, then the mixture was extracted with ethyl acetate (4×100 mL). The organic layers were dried with MgSO4 and evaporated to a solid that weighed 10.5 g. The residue was dissolved in 400 mL boiling ethyl acetate, the insoluble material was filtered away and the filtrate was evaporated. 7-bromo-5-chloro-1H-indole-3-carbaldehyde (6.45 g, 24.95 mmol, 82% yield) was obtained as an off-white solid. 1H-NMR (CDCl3, 400 MHz) δ 9.99 (s, 1H), 8.35 (s, 1H), 8.32 (s, 1H), 7.92 (s, 1H), 7.47 (d, J=2.0 Hz, 1H). LC/MS (HPLC method 4): tR=2.87 min, 257.91(MH)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08026257B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-e8ac9ee96e52429c9f40f89914f50e29
Quellennotizuspto-grants-2011_09