HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718501Generated: October 30, 2026
Tetrahydrofuran → 4-Ethoxy-3-fluoro-2-formylphenylboronic acid
https://huagongshe.com/reaction/718501
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 2-(6-Bromo-2-fluoro-3-propylphenyl)-1,3-dioxolane | HCID 86696073 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 4-Ethoxy-3-fluoro-2-formylphenylboronic acid | HCID 46918610 | 86% |
Reaction Steps
Under a nitrogen atmosphere, n-BuLi (141.1 mL, 232.8 mmol) was slowly added dropwise, at −70° C. or lower, to a THF (500 mL) solution of compound (78) (61.2 g, 213.0 mmol). The reaction mixture was agitated at −70° C. or lower for 1 hour, and then trimethyl borate (33.0 g, 317 mmol) was slowly added dropwise thereto. The reaction mixture was returned to room temperature, and then quenched with 400 mL of 2N hydrochloric acid aqueous solution, and extracted with 200 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 (3-fluoro-2-formyl-4-ethoxyphenyl)boronic acid (79) (38.1 g, yield 86.0%) 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-9c4b1f65f4da4500b066d80c3b9f3ca0 |
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| Source note | uspto-grants-2015_11 |
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