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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 73930Erstellt: 25. Oktober 2026

t-Butyl bromide → 3-(tert-Butyl)-6-nitro-1h-indole

https://huagongshe.com/reaction/73930

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktt-Butyl bromideHCID 10485—
Edukt6-Nitro-1H-indoleHCID 78502—
EduktDiisopropylethylamineHCID 81531—
KatalysatorTetrabutylammonium IodideHCID 67553—
KatalysatorZinc trifluoromethanesulfonateHCID 104671—
LösungsmittelTolueneHCID 1140—
Produkt3-(tert-Butyl)-6-nitro-1h-indoleHCID 5747019822,2%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To a mixture of 6-nitroindole (1 g, 6.2 mmol), zinc triflate (2.06 g, 5.7 mmol) and TBAI (1.7 g, 5.16 mmol) in anhydrous toluene (11 mL) was added DIEA (1.47 g, 11.4 mmol) at room temperature under nitrogen. The reaction mixture was stirred for 10 min at 120° C., followed by addition of t-butyl bromide (0.707 g, 5.16 mmol). The resulting mixture was stirred for 45 min at 120° C. The solid was filtered off and the filtrate was concentrated to dryness and purified by column chromatography on silica gel (Pet.Ether./EtOAc 20:1) to give 3-tert-butyl-6-nitro-1H-indole as a yellow solid (0.25 g, 19%). 1H NMR (CDCl3) δ 8.32 (d, J=2.1 Hz, 1H), 8.00 (dd, J=2.1, 14.4 Hz, 1H), 7.85 (d, J=8.7 Hz, 1H), 7.25 (s, 1H), 1.46 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829204B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-f2ad71930ecb4773ba351e9d93c9dc4e
Quellennotizuspto-grants-2014_09