HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537959Generated: October 26, 2026
Trimethyl borate → (4-Fluoro-5-isopropyl-2-methoxyphenyl)boronic acid
https://huagongshe.com/reaction/537959
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1-Fluoro-4-iodo-2-isopropyl-5-methoxybenzene | HCID 53363741 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Fluoro-5-isopropyl-2-methoxyphenyl)boronic acid | HCID 53363739 | — |
Reaction Steps
To a solution of 1-fluoro-4-iodo-2-isopropyl-5-methoxybenzene (Intermediate 5, 2.61 g, 8.88 mmol) in THF at −78° C., n-BuLi (4.26 mL, 10.65 mmol, 2.5 M) was added dropwise. The solution was stirred at −78° C. for 30 min. Trimethyl borate (2.98 mL, 26.6 mmol) was added. The solution was then stirred at −78° C. for 3 h. The reaction was quenched at −78° C. with saturated ammonium chloride and the mixture was warmed to room temperature. The organic layer was extracted with ethyl acetate (3×50 mL). The combined ethyl acetate layers were washed with brine and dried over sodium sulfate. The title compound was obtained as a white solid. 1H NMR (CDCl3, 500 MHz) δ 7.74 (d, J=10.0 Hz, 1H), 6.62 (d, J=12.5 Hz, 1H), 5.65 (br s, 2H), 3.92 (s, 3H), 3.20 (m, 1H), 1.22 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865707B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-f1619c462d3c49e594e45729ac5dce08 |
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| Source note | uspto-grants-2014_10 |
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