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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68698Generated: October 25, 2026

Boric acid (H3BO3), tripropyl ester → 3-ethyl-1-phenyl-1H-indazol-6-ylboronic acid

https://huagongshe.com/reaction/68698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoric acid (H3BO3), tripropyl esterHCID 12711—
Reactant6-bromo-3-ethyl-1-phenyl-1H-indazoleHCID 67449468—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-ethyl-1-phenyl-1H-indazol-6-ylboronic acidHCID 67448555—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Into a 250-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 6-bromo-3-ethyl-1-phenyl-1H-indazole (2 g, 6.64 mmol, 1.00 equiv) in tetrahydrofuran (20 mL). To the resulting mixture was then added a solution of n-BuLi (4 mL, 1.40 equiv) in tetrahydrofuran (5 mL) dropwise with stirring at −78° C. in 5 min. The resulting mixture was stirred for 30 min at the temperature. To the resulting mixture was then added a solution of tripropyl borate (1.49 g, 7.93 mmol, 1.20 equiv) in tetrahydrofuran (5 mL) dropwise with stirring at −78° C. in 5 min. The resulting solution was stirred for 1 h at −78° C. in a liquid nitrogen bath. The reaction was then quenched by the addition of water (30 mL). The resulting solution was extracted with ethyl acetate (2×50 mL), the organic layers combined and dried over anhydrous sodium sulfate, then concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:5) to yield 3-ethyl-1-phenyl-1H-indazol-6-ylboronic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822447B2
Source datasetuspto-grants-2014_09
ORD IDord-98d695e364564352833374340912d32e
Source noteuspto-grants-2014_09