Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167203Generated: November 2, 2026

Triisopropyl borate → 2-Fluorophenylboronic acid

https://huagongshe.com/reaction/1167203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant1-Bromo-2-fluorobenzeneHCID 61259—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Fluorophenylboronic acidHCID 273435463.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 50 g (285.6 mmol) of 2-fluorobromobenzene in 400 mL of tetrahydrofuran was cooled to −78° C. and 200 mL (320.0 mmol) of 1.6M n-Butyllithium was added via a cannula. The mixture was stirred at −78° C. for 60 minutes, then 98.9 mL (428.4 mmol) of triisopropyl borate was added via a cannula and stirring was continued for 60 minutes. The cooling bath was removed and the mixture was stirred at ambient temperature for 1.5 hours, then 150 mL of 6N hydrochloric acid was added and stirring was continued for 1.5 hours. To the mixture was added 100 mL of brine, and then the organic layer was separated and the aqueous layer was extracted three times with 30 mL each of ether. The combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo. The residue was recrystallized from water to afford 25.2 g (63%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617351B1
Source datasetuspto-grants-2003_09
ORD IDord-4ff4fb95a88d499891cf9a267ac8b82a
Source noteuspto-grants-2003_09