戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 895673作成日:2026年10月25日

Potassium Nitrate → 4-Bromo-5-nitroisoquinoline

https://huagongshe.com/reaction/895673

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium NitrateHCID 24434—
反応物4-BromoisoquinolineHCID 73743—
反応物2-(3,4-Dimethoxy-2-methoxymethoxyphenyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolaneHCID 22380772—
溶媒Sulfuric AcidHCID 1118—
生成物4-Bromo-5-nitroisoquinolineHCID 271280—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06916832B2
出典データセットuspto-grants-2005_07
ORD IDord-e085fb8b699049ba854c3f8b8b913c33
出典メモuspto-grants-2005_07