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HRID 1748714作成日:2026年10月25日

Trimethylsilyldiazomethane → Methyl 4-bromopicolinate

https://huagongshe.com/reaction/1748714

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilyldiazomethaneHCID 167693—
反応物4-Bromopyridine-2-carboxylic acidHCID 735150—
溶媒MethanolHCID 887—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 4-bromopicolinateHCID 1282894773%

反応手順

To a solution of 4-bromopyridine-2-carboxylic acid (0.5 g, 2.5 mmol, Apollo Scientific) in a mixture of ethyl acetate (15 mL) and methanol (1.5 mL), was added dropwise a solution of trimethylsilyldiazomethane (3.7 mL, 2 M in diethyl ether, 7.4 mmol), at about 0° C. After the addition was complete the temperature was raised to rt and the mixture stirred for about another 1.5 h at rt. The resulting mixture was concentrated in vacuo and diethyl ether (25 mL) was added to the residue. The resulting mixture was filtered and concentrated in vacuo. The residue was purified by column chromatography (SiO2, diethyl ether/hexanes 1:1) to give methyl 4-bromopyridine-2-carboxylate (0.39 g, 1.8 mmol, 73%) as a pale yellow solid: 1H-NMR (CDCl3, Bruker 400 MHz) δ 4.03 (3H, s), 7.67 (1H, dd, J=5.0, 1.6 Hz), 8.31 (1H, d, J=1.6 Hz), 8.57 (1H, d, J=5.0 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09150592B2
出典データセットuspto-grants-2015_10
ORD IDord-66b5011882ef4d179eb52ffe091205e8
出典メモuspto-grants-2015_10