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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 7-Bromo-4,5-difluorobenzofuran | HCID 22144874 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4,5-Difluorobenzofuran-7-yl)boronic acid | HCID 22495642 | 123.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06881733B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-58a866e078714fc9b144d3a8df6cd6e9 |
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| Source note | uspto-grants-2005_04 |
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