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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895673Generated: October 25, 2026

Potassium Nitrate → 4-Bromo-5-nitroisoquinoline

https://huagongshe.com/reaction/895673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
Reactant4-BromoisoquinolineHCID 73743—
Reactant2-(3,4-Dimethoxy-2-methoxymethoxyphenyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolaneHCID 22380772—
SolventSulfuric AcidHCID 1118—
Product4-Bromo-5-nitroisoquinolineHCID 271280—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916832B2
Source datasetuspto-grants-2005_07
ORD IDord-e085fb8b699049ba854c3f8b8b913c33
Source noteuspto-grants-2005_07