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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178989Generated: October 29, 2026

Water → Phenylboronic Acid

https://huagongshe.com/reaction/2178989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
ReactantButyllithiumHCID 178418339—
ProductPhenylboronic AcidHCID 66827—

Reaction Steps

In an Ar atmosphere, the crystals of 2-(4-bromophenyl)-naphthalene obtained in Synthesis Step C1-3, 10 g, and 500 mL of anhydrous tetrahydrofuran were put into a 1-L flask, and then 22 mL of a 1.6 M n-BuLi solution in hexane was added dropwise at −60° C. over 30 minutes. Thirty minutes later, 7 g of triisopropyl borate was added dropwise, and then the reaction was allowed to proceed overnight with no temperature control. After the completion of the reaction, 100 mL of water was added dropwise, and the obtained solution was subjected to extraction with 2 L of toluene and separated. The isolated organic layer was concentrated, the residue was recrystallized, and the crystals were collected by filtration and dried. In this way, a phenylboronic acid derivative was obtained as a white solid weighing 5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067952B2
Source datasetuspto-grants-2015_06
ORD IDord-25221e0603cb4c0c9382b57ea8c498fa
Source noteuspto-grants-2015_06