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HRID 1811802생성일: 2026년 10월 27일

Tetrahydrofuran → 2-Chloro-5-methoxypyridine-3-boronic acid

https://huagongshe.com/reaction/1811802

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물HexaneHCID 8058—
반응물Triisopropyl borateHCID 21531—
반응물3-Bromo-2-chloro-5-methoxypyridineHCID 46738814—
반응물ButyllithiumHCID 178418339—
생성물2-Chloro-5-methoxypyridine-3-boronic acidHCID 4673881671%

반응 단계

2.5 M n-BuLi in hexane (3.7 mL, 9.3 mmol) was added slowly to a stirred premixed solution of 3-bromo-2-chloro-5-methoxypyridine (1.73 g, 7.8 mmol) and triisopropyl borate (2.1 mL, 9.3 mmol) in THF (10.0 mL, 122 mmol) at −78° C., and the resulting deep colored mixture was stirred at the same temperature for 1 h and then allowed to warm up to room temperature over 1 h. The reaction was quenched with 1 N NaOH(aq) and then some EtOAc. The separated aqueous layer was acidified with 5 N HCl until pH about 5 and then extracted with EtOAc (×2) and the combined organic layers were washed with brine, dried over Na2SO4, and concentrated to give 2-chloro-5-methoxypyridin-3-ylboronic acid (1.0276 g, 71%) as a brown solid. LCMS (API-ES) m/z 188 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362241B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-e1d66a59d13a47ceb838142b9a59ceb4
출처 메모uspto-grants-2013_01