Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718501Generated: October 30, 2026

Tetrahydrofuran → 4-Ethoxy-3-fluoro-2-formylphenylboronic acid

https://huagongshe.com/reaction/718501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTrimethyl borateHCID 8470—
Reactant2-(6-Bromo-2-fluoro-3-propylphenyl)-1,3-dioxolaneHCID 86696073—
ReactantButyllithiumHCID 178418339—
Product4-Ethoxy-3-fluoro-2-formylphenylboronic acidHCID 4691861086%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Under a nitrogen atmosphere, n-BuLi (141.1 mL, 232.8 mmol) was slowly added dropwise, at −70° C. or lower, to a THF (500 mL) solution of compound (78) (61.2 g, 213.0 mmol). The reaction mixture was agitated at −70° C. or lower for 1 hour, and then trimethyl borate (33.0 g, 317 mmol) was slowly added dropwise thereto. The reaction mixture was returned to room temperature, and then quenched with 400 mL of 2N hydrochloric acid aqueous solution, and extracted with 200 mL of toluene three times. Combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate, water and saturated brine, and then dried over magnesium sulfate, and a solvent was distilled off by an evaporator. The residue was washed with heptane, and thus (3-fluoro-2-formyl-4-ethoxyphenyl)boronic acid (79) (38.1 g, yield 86.0%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193908B2
Source datasetuspto-grants-2015_11
ORD IDord-9c4b1f65f4da4500b066d80c3b9f3ca0
Source noteuspto-grants-2015_11