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HRID 1782581作成日:2026年10月27日

Bromine → 2,3-Dibromo-4-methylpyridine

https://huagongshe.com/reaction/1782581

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物3-Bromo-4-methylpyridin-2-amineHCID 14418043—
反応物Sodium NitriteHCID 23668193—
溶媒Hydrogen BromideHCID 260—
溶媒WaterHCID 962—
生成物2,3-Dibromo-4-methylpyridineHCID 2230869547%

反応条件

温度10 °C

反応手順

Bromine (0.35 mL, 6.8 mmol) was added dropwise to a solution of 3-bromo-4-methyl-pyridin-2-ylamine (0.44 g, 2.4 mmol) in 48% HBr (3 mL) at −10° C. to give an orange slurry. After 5 minutes NaNO2 (0.47 g, 6.8 mmol), dissolved in water (1.5 mL), was added dropwise over 5 minutes. The dark brown mixture was slowly warmed to 10° C. over 3.5 h and then cooled to 0° C. and quenched with 10N NaOH until pH˜12. The resulting orange slurry was extracted with CH2Cl2 (3×50 mL), dried (Na2SO4), filtered and concentrated in vacuo to give an orange/brown solid. Purification by column chromatography on silica gel (Hexanes:Et2O, 7:3, v/v) yielded 2,3-dibromo-4-methyl-pyridine (0.28 g, 47%) as a pale yellow solid. 1H NMR (CDCl3) δ 2.48 (s, 3H), 7.11 (d, 1H, J=6.0 Hz), 8.16 (d, 1H, J=6.0 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07498346B2
出典データセットuspto-grants-2009_03
ORD IDord-f5e070cde61946ea91f96e687bae81a4
出典メモuspto-grants-2009_03