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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598001생성일: 2026년 10월 27일

Hydrochloric Acid → 5-Methoxypyridine-3-boronic Acid

https://huagongshe.com/reaction/598001

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Triisopropyl borateHCID 21531—
반응물3-Bromo-5-methoxypyridineHCID 817163—
반응물ButyllithiumHCID 178418339—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물5-Methoxypyridine-3-boronic AcidHCID 276308794.4%

반응 조건

온도-40 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897611B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-f6e7b22a00b546fd990f9e53c1400b4c
출처 메모uspto-grants-2011_03