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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216183Generated: October 25, 2026

Triisopropyl borate → 2-(5-borono-1H-indol-3-yl)acetic acid

https://huagongshe.com/reaction/216183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant5-Bromo-3-indoleacetic acidHCID 96734—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product2-(5-borono-1H-indol-3-yl)acetic acidHCID 5763607821.4%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of (5-bromo-1H-indol-3-yl)-acetic acid (1 g, 3.94 mmol) in THF (66 mL) at −78° C. is added tert-butyl lithium (1.7 M in pentane, 11.6 mL, 19.7 mmol) dropwise and stirred at −78° C. for 30 minutes at −30° C. for 1 hour. Cooled down to −78° C. again and treated dropwise with triisopropyl borate (4.53 mL, 19.7 mmol). The reaction mixture is allowed to warm to room temperature during 1 hour quenched with 2N hydrochloric acid. This mixture is extracted with ether. The extract is dried over sodium sulfate and concentrate to obtain an oil which is subjected to silica gel chromatography affording 3-carboxymethyl-1H-indol-5-yl boronic acid (185 mg, 20%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193183B2
Source datasetuspto-grants-2012_06
ORD IDord-79c8e14816874338911ae4501bb00c4f
Source noteuspto-grants-2012_06