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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815828Generated: October 26, 2026

Trimethyl borate → (4,5-Difluorobenzofuran-7-yl)boronic acid

https://huagongshe.com/reaction/1815828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantMagnesiumHCID 5462224—
Reactant7-Bromo-4,5-difluorobenzofuranHCID 22144874—
SolventTetrahydrofuranHCID 8028—
Product(4,5-Difluorobenzofuran-7-yl)boronic acidHCID 22495642123.7%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A mixture of 2.0 gm (8.58mMol) 4,5-difluoro-7-bromobenzofuran and 0.202 gm (8.58 mMol) magnesium in 10 mL tetrahydrofuran was heated at reflux for 50 minutes. The resulting mixture was then cooled to −5° C. and treated dropwise with 1.01 mL (8.93 mMol) trimethylborate over 20 minutes. The reaction mixture was stirred at room temperature for 1.5 hours and was then concentrated under reduced pressure. The residue was partitioned between 50 mL deionized water and 50 mL ethyl acetate. The mixture was treated with 0.3 mL acetic acid to adjust to a neutral pH. The phases were separated and the aqueous phase was extracted well with ethyl acetate. The organic phases were combined, dried over magnesium sulfate, and concentrated under reduced pressure to provide 2.1 gm of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881733B1
Source datasetuspto-grants-2005_04
ORD IDord-58a866e078714fc9b144d3a8df6cd6e9
Source noteuspto-grants-2005_04