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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571446Generated: November 1, 2026

tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate → 1-(tert-Butoxycarbonyl)-1H-indole-5-boronic acid

https://huagongshe.com/reaction/571446

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylateHCID 2757340—
SolventPropan-2-one--water (1/1)HCID 18366337—
Product1-(tert-Butoxycarbonyl)-1H-indole-5-boronic acidHCID 1837563754%

Reaction Conditions

Temperature23 °C

Reaction Steps

To N-Boc-indole-5-boronic acid pinacol ester (172 mg, 0.500 mmol, 1.00 equiv) in acetone/H2O (5.0 mL/5.0 mL) at 23° C. was added NH4OAc (193 mg, 2.50 mmol, 5.00 equiv) and NaIO4 (535 mg, 2.00 mmol, 4.00 equiv). After stirring for 24 hr at 23° C., the reaction mixture was concentrated in vacuo to remove acetone. To the residual solution was added EtOAc (5 mL) and the phases were separated. The aqueous phase was extracted with EtOAc (2×5 mL). The combined organic phases are washed with brine (10 mL) and dried (Na2SO4). The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica gel eluting with hexanes/EtOAc 1:1 (v/v) to afford 70.0 mg of the title compound as a colorless solid (54% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024093B2
Source datasetuspto-grants-2015_05
ORD IDord-5f8ace77f2db4ec0a5c460ccb8b655f7
Source noteuspto-grants-2015_05