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HRID 1517014作成日:2026年10月25日

Hydrogen Bromide → 5-Bromo-2-methylbenzothiazole

https://huagongshe.com/reaction/1517014

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物WaterHCID 962—
反応物Ammonium HydroxideHCID 14923—
反応物2-Methylbenzothiazol-5-ylamine dihydrochlorideHCID 16218943—
反応物Sodium NitriteHCID 23668193—
触媒copper(I) bromideHCID 24593—
生成物5-Bromo-2-methylbenzothiazoleHCID 3017457—

反応条件

温度0 °C

反応手順

Sodium nitrite (0.9 g, 13 mmol) was added portionwise to a suspension of 2-methyl-5-aminobenzothiazole dihydrochloride (2.0 g, 8 mmol) in hydrobromic acid (24 ml) at 0° C. The resulting mixture was added dropwise to a solution of copper(I) bromide (4.0 g, 14 mmol) in hydrobromic acid (50 ml) at 0° C. After stirring at 0° C. for 2 hours, water was added. The reaction mixture was basified to pH 9 using aqueous ammonium hydroxide and was extracted with ethyl acetate. The combined organic layers were dried over magnesium sulfate to give 2-methyl-5-bromobenzothiazole (1.0 g, 52%, 82% AUC GC) after chromatography (9:1 heptane/ethyl acetate): 1H NMR (300 MHz, DMSO-d6) δ 8.12 (d, J=1.8 Hz, 8.02 (dd, 1H) J=8.4, 1.5 Hz, 1H), 7.56 (dd, J=8.7, 2. Hz, 1H), 2.81 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08227486B2
出典データセットuspto-grants-2012_07
ORD IDord-d059c31b525c4b3a9b7d9de4e8774d84
出典メモuspto-grants-2012_07