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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025287Generated: October 26, 2026

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

https://huagongshe.com/reaction/1025287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIndoleHCID 798—
ReactantTriisopropyl borateHCID 21531—
ReactantSodium BicarbonateHCID 516892—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1H-Indol-2-ylboronic acidHCID 2256735831.1%

Reaction Conditions

Temperature-40 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729071B2
Source datasetuspto-grants-2014_05
ORD IDord-a287b6ed2e6c44d996e6c6da898ea065
Source noteuspto-grants-2014_05