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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403367Generated: October 31, 2026

Triisopropyl borate → (1-Benzofuran-5-yl)boronic acid

https://huagongshe.com/reaction/1403367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
ReactantBenzofuran, 5-bromo-HCID 90015—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(1-Benzofuran-5-yl)boronic acidHCID 419799960.8%

Reaction Conditions

Temperature-30 °C

Reaction Steps

The solution of 5-bromo-1-benzofuran (1.0 g, 5.08 mmol) in dry tetrahydrofuran (50 mL) was kept below −60° C. under nitrogen, while BuLi (6.09 mmol, 2.5M solution in hexane) was added dropwise. It was warmed to −30° C. during 45 min and stirred at this temperature for another 30 min. The mixture was cooled again below −60° C. followed by dropwise addition of triisopropyl borate (1.44 g, 7.66 mmol). After warming to room temperature the mixture was quenched with hydrochloric acid (30 mL, 2N) and stirred for 1 h. The alkaline aqueous layer was brought to pH 5 and extracted with ethyl acetate (3×80 mL). All organic layers were combined, dried over sodium sulfate, and concentrated in vacuo to give (1-benzofuran-5-yl)boronic acid (500 mg, crude), which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-2fba19769b44472da35c4f39c20a41ae
Source noteuspto-grants-2014_12