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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1429698Erstellt: 25. Oktober 2026

Hydrochloric Acid → 1H-Indol-2-ylboronic acid

https://huagongshe.com/reaction/1429698

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIndoleHCID 798—
EduktTriisopropyl borateHCID 21531—
EduktSodium BicarbonateHCID 516892—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1H-Indol-2-ylboronic acidHCID 2256735831,1%

Reaktionsbedingungen

Temperatur-40 °C

Reaktionsschritte

To the SEM-protected indole prepared in step 1 (0.99 g, 4.0 mmol) in THF (10 mL) at −40° C. was added n-BuLi (2.5 M in hexanes, 1.9 mL, 4.8 mmol). The mixture was stirred at −40° C. for 1 h and then triisopropyl borate (1.2 mL, 5.2 mmol) was added. The mixture was allowed to warm to room temperature while stirring for 18 h. To the reaction mixture was added 1N HCl (aq). The mixture was stirred at room temperature for 30 minutes. The mixture was then adjusted to pH˜5 using saturated NaHCO3 (aq) The mixture was extracted with ether. The combined ether extracts were washed with water and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (0-50% EtOAc/hex over 30 minutes) to provide the indole boronic acid (0.20 g, 17%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08940748B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-5043e3e05b6c4269bdc552cc0374bbc6
Quellennotizuspto-grants-2015_01