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HRID 530017作成日:2026年10月27日

Diethyl Ether → 2-(5-Bromo-3-pyridyl)propan-2-ol

https://huagongshe.com/reaction/530017

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物3-Acetyl-5-bromopyridineHCID 820423—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
生成物2-(5-Bromo-3-pyridyl)propan-2-olHCID 22391966—

反応手順

To a cooled (−78° C.) solution of 3-acetyl-5-bromo pyridine (1.98 g, 9.90 mmol) in tetrahydrofuran (33 mL) was added dropwise a solution of methyl magnesium bromide in diethyl ether (3.0 M, 6.60 mL, 19.8 mmol). The reaction was warmed to room temperature, and the resulting mixture was stirred at room temperature overnight. The reaction was then quenched with saturated aqueous ammonium chloride solution and extracted with diethyl ether. The organic extracts were combined, washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by flash chromatography on silica gel (0-60% ethyl acetate in hexanes) provided the title compound: LCMS m/z 217.83 [M+H]+; 1H NMR (500 MHz, CDCl3) δ 8.61 (s, 1 H), 8.53 (s, 1 H), 8.01 (d, J=1.9 Hz, 1 H), 2.38 (br s, 1 H), 1.61 (6 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09351973B2
出典データセットuspto-grants-2016_05
ORD IDord-9d68144ca2c048fe9759be13c9ba3edc
出典メモuspto-grants-2016_05