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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 895673Erstellt: 23. Oktober 2026

Potassium Nitrate → 4-Bromo-5-nitroisoquinoline

https://huagongshe.com/de/reaction/895673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium NitrateHCID 24434—
Edukt4-BromoisoquinolineHCID 73743—
Edukt2-(3,4-Dimethoxy-2-methoxymethoxyphenyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolaneHCID 22380772—
LösungsmittelSulfuric AcidHCID 1118—
Produkt4-Bromo-5-nitroisoquinolineHCID 271280—

Reaktionsschritte

Potassium nitrate (5.34 g; 0.052 mol) was added to 20 ml of concentrated sulfuric acid and slowly dissolved by careful heating. The resulting solution was added dropwise to a solution of 4-bromoisoquinoline (10 g; 0.048 mol) dissolved in 40 ml of the same acid at 0° C. After removal of the cooling bath, the solution was stirred for one hour at room temperature. The reaction mixture was then poured onto crushed ice (400 g) and made basic with ammonium hydroxide. The resulting yellow precipitate was collected by filtration and the filtrate was extracted with diethyl ether (3×500 ml), dried (Na2SO4), and concentrated to give a yellow solid that was combined with the initial precipitate. Recrystallization from methanol gave 12.1 g (89%) of slightly yellow crystals: mp 172-174° C.; 1H NMR: (300 MHz, CDCl3): 9.27 (s, 1H); 8.87 (s, 1H); 8.21 (dd, 1H, J=6.6, 1.2 Hz); 7.96 (dd, 1H, J=6.6, 1.2 Hz); 7.73 (t, 1H, J=7.5 Hz). CIMS m/z: 253 (M+H+, 100%); 255 (M+H++2, 100%). Anal. Calc'd for C9H5BrN2O2: C, 42.72; H, 1.99; N, 11.07. Found: C, 42.59; H, 1.76; N, 10.87.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06916832B2
Quelldatensatzuspto-grants-2005_07
ORD IDord-e085fb8b699049ba854c3f8b8b913c33
Quellennotizuspto-grants-2005_07