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HRID 1176757作成日:2026年10月27日

N-bromobutanimide → Methyl 6-(bromomethyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/1176757

反応式

関与物質

役割名称HCID仕込み量
反応物N-bromobutanimideHCID 67184—
反応物Methyl 6-methylpyridine-2-carboxylateHCID 73022—
触媒Benzoyl PeroxideHCID 7187—
溶媒Carbon TetrachlorideHCID 5943—
生成物Methyl 6-(bromomethyl)pyridine-2-carboxylateHCID 2147171420.2%

反応手順

6-Bromomethyl-pyridine-2-carboxylic acid methyl ester was prepared according to Wells, G. J. et al. (WO 94/11398): A mixture of 6-methyl-pyridine-2-carboxylic acid methyl ester (6.5 g, 43.0 mmol), benzoyl peroxide (25 mg, 0.1 mmol) and NBS (8.5 g, 47.8 mmol) in carbon tetrachloride (250 mL) was heated at reflux overnight. The reaction mixture was cooled to room temperature, filtered, evaporated, and purified by chromatography on flash silica gel, eluting with 15% ethyl acetate/hexane to give 6-bromomethyl-pyridine-2-carboxylic acid methyl ester (2.0 g, 20%) as a white solid. 1HNMR (CDCl3): δ 8.06 (d, J=8.0 Hz, 1H), 7.87 (dd, J=8.0 Hz, 1H), 7.70 (d, J=8.0 Hz, 1H), 4.65 (s, 2H), 4.02 (s, 3H). MS (APCI+): 231 (45), 235 (42).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07842825B2
出典データセットuspto-grants-2010_11
ORD IDord-d9673c2fb2bc45969f422b986ec8dc57
出典メモuspto-grants-2010_11