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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 598001Erstellt: 26. Oktober 2026

Hydrochloric Acid → 5-Methoxypyridine-3-boronic Acid

https://huagongshe.com/reaction/598001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriisopropyl borateHCID 21531—
Edukt3-Bromo-5-methoxypyridineHCID 817163—
EduktButyllithiumHCID 178418339—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Methoxypyridine-3-boronic AcidHCID 276308794,4%

Reaktionsbedingungen

Temperatur-40 °C

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07897611B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-f6e7b22a00b546fd990f9e53c1400b4c
Quellennotizuspto-grants-2011_03