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HRID 598001作成日:2026年10月27日

Hydrochloric Acid → 5-Methoxypyridine-3-boronic Acid

https://huagongshe.com/reaction/598001

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Triisopropyl borateHCID 21531—
反応物3-Bromo-5-methoxypyridineHCID 817163—
反応物ButyllithiumHCID 178418339—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物5-Methoxypyridine-3-boronic AcidHCID 276308794.4%

反応条件

温度-40 °C

反応手順

Triisopropyl borate (29.3 mL, 128 mmol) was added over 2 min to a solution of 5-methoxy-3-bromopyridine (20.00 g, 106.4 mmol) in toluene (140 mL) and tetrahydrofuran (35 mL) at −40° C. To this solution was added 2.5 M n-BuLi (51.1 mL, 128 mmol) drop-wise over 35 min while maintaining the temperature at −40° C. After the addition was complete, the reaction was stirred an additional 30 min at −40° C. and then was warmed to −15° C. over one hour. Into the reaction was poured 1 N HCl (175 mL), and the mixture was stirred vigorously for 30 minutes. The layers were separated, and the organic washed once with water (15 mL). The aqueous phases were combined and neutralized (to pH 7) with 5 N NaOH, at which point the boronic acid precipitated out. The biphasic mixture was extracted with THF (3×150 mL). The organic phases were combined, dried over sodium sulfate, filtered, and concentrated to yield 15.36 g of 5-methoxy-3-pyridinylboronic acid as a light brown solid (94%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07897611B2
出典データセットuspto-grants-2011_03
ORD IDord-f6e7b22a00b546fd990f9e53c1400b4c
出典メモuspto-grants-2011_03