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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72271Generated: October 27, 2026

Trimethyl borate → 5-Bromo-2-chlorophenylboronic acid

https://huagongshe.com/reaction/72271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant4-Bromo-1-chloro-2-iodobenzeneHCID 51000071—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-chlorophenylboronic acidHCID 4673681679.3%

Reaction Conditions

Temperature-75 °C

Reaction Steps

4-Bromo-1-chloro-2-iodobenzene (10.35 g, 33 mmol) is dissolved in anhydrous tetrahydrofuran (60 ml) and the solution is cooled to −75° C. under an atmosphere of argon. Isopropylmagnesium chloride (17.1 ml, 34 mmol, 2M solution in tetrahydrofuran) is added dropwise over 30 minutes, maintaining the internal temperature below −70° C. by external cooling. Once the addition is complete, the reaction mixture is stirred at approximately −70° C. for 30 minutes and then allowed to warm to room temperature and stirred for 1 hour. The reaction mixture is then cooled to −78° C. and trimethyl borate (7.3 ml, 65 mmol) is added dropwise. The mixture is stirred at −78° C. for 30 minutes and then the cooling bath is removed and the mixture is stirred at room temperature for 1.5 hours. 2M Aqueous hydrochloric acid (30 ml) is added, and the crude product is extracted with ethyl acetate. The organic phase is washed with water and brine, dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated in vacuo. Trituration with hexane gives 5-bromo-2-chlorophenylboronic acid (6.16 g) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828908B2
Source datasetuspto-grants-2014_09
ORD IDord-32389e2238464edc91c2cbfc2098ed62
Source noteuspto-grants-2014_09