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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718484Generated: October 28, 2026

Trimethyl borate → 4-Ethoxy-3-fluoro-2-formylphenylboronic acid

https://huagongshe.com/reaction/718484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant2-(2-Bromo-6-fluoro-5-ethoxyphenyl)-1,3-dioxolaneHCID 68010537—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Ethoxy-3-fluoro-2-formylphenylboronic acidHCID 4691861068.3%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Under a nitrogen atmosphere, n-BuLi (43.3 mL, 71.42 mmol) was slowly added dropwise, at −70° C. or lower, to a THF (200 mL) solution of compound (54) (19.8 g, 68.02 mmol). The reaction mixture was agitated at −70° C. or lower for 1 hour, and then trimethyl borate (10.6 g, 102.0 mmol) was slowly added dropwise thereto. The reaction mixture was returned to room temperature, and then quenched with 200 mL of 2N hydrochloric acid aqueous solution, and extracted with 100 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 (4-ethoxy-3-fluoro-2-formylphenyl)boronic acid (55) (9.85 g, yield 68.3%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193908B2
Source datasetuspto-grants-2015_11
ORD IDord-8f159497c2f04ec197d2f92f54293010
Source noteuspto-grants-2015_11