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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 2-(2-Bromo-6-fluoro-5-ethoxyphenyl)-1,3-dioxolane | HCID 68010537 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Ethoxy-3-fluoro-2-formylphenylboronic acid | HCID 46918610 | 68.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193908B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-8f159497c2f04ec197d2f92f54293010 |
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| Source note | uspto-grants-2015_11 |
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